373 Medical Internship jobs in India
Medical Advisor/Senior Medical Advisor
Mumbai, Maharashtra
Alkem Laboratories Ltd.
Posted 5 days ago
Job Viewed
Job Description
About Alkem:
Alkem Laboratories Limited is an Indian multinational pharmaceutical company headquartered in Mumbai, that manufactures and sells pharmaceutical generics, formulations and nutraceuticals in India and globally over 50 countries. We have consistently been ranked amongst the five pharmaceutical companies in India. Our portfolio includes illustrious brands like Clavam, Pan, Pan-D, and Taxim-O, which feature amongst the top 50 pharmaceutical brands in India.
Job Purpose:
- To actively contribute to the organization/division by taking responsibility for the scientific, technical and ethical soundness of all policies, statements and endeavors.
- To support the division medically in all activities related to the portfolio and provide high quality and timely service to internal and external stake holders.
Responsibilities:
- To actively support development of promotion of allocated portfolio under supervision from the Line manager or the mentor, provide strategic inputs and support towards creation of marketing/brand plans/medical development plans, and towards design and execution of medical-marketing programs/clinical programs, including initiatives to enhance access to medicines
- Under supervision from the Line manager or mentor, create/review promotional, training, and Continuing Medical Education (CME) material in compliance with relevant industry codes and medical correctness
- In consultation with the Line manager or mentor, participate/facilitate/conduct customized promotional/educational interactions with Key Opinion Leaders (KOLs). These interactions include, but are not limited to, customer launch meetings, advisory boards, CME programs, scientific symposia, institutional presentations, medical projects and studies
- In consultation with concerned stakeholders plan research projects and develop / review / approve protocol synopsis/final protocols/supporting documents per need
- Provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external (HCPs) customers, in adherence to relevant SOPs/policies
- Impart medical training to new sales staff on basic sciences/ TAs/assigned products. Provide refresher training to sales staff through ongoing training initiatives. Provide pre-launch and launch training to sales staff for new products
- Support New Product Evaluation (NPE), Marketing, and Business Development colleagues with medical evaluation and recommendations on commercial opportunities with new products. Support organization efforts at developing local formulations/line extensions through literature search/recommendations
- Support regulatory team by means of writing/revising/reviewing labeling documents for products as per relevant SOPs
- Support Pharmacovigilance activities by documentation and reporting of Adverse Events in a timely manner.
Qualification : MBBS & MD Pharmacology (Mandatory)
Experience : 1 to 4 years of experience in medico marketing
This advertiser has chosen not to accept applicants from your region.
0
Senior Medical Writer, Medical Communications
Cactus Life Sciences
Posted 5 days ago
Job Viewed
Job Description
Overview:
Please Note: You may be required to travel to our Mumbai office based on business requirements or for company/team events.
If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Senior Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you.
Job Responsibilities:
- Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client needs with excellent attention to detail under the guidance of the scientific leads
- Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas -- learning to anticipate their needs
- Effectively and proactively communicate with team members, authors/faculty, clients and vendors
- Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives
- Attend client and other external meetings and supporting senior team members as needed
- Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans
- You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date.
- Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines
- Share best practices and client preferences, thereby contributing to skill development within the medical communications team
Requirements:
- 3-5 years of experience in relevant fields of scientific writing
- PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD with a good understanding of clinical research and medical communication
- Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills
- Excellent communication skills, especially with the clients
- Ability to adapt writing style to different materials and target audiences
- Basic knowledge of biostatistics
- Literature reviewing and evaluation capabilities
- Very good working knowledge of MS Office
Application Process:
Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds.
Equal Opportunity
Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic.
Accelerating from Anywhere
As a remote-first organization, these are essential attributes we look for in all our candidates.
- Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently.
- Documenting work that brings everyone on the same page.
- Maturity to choose between synchronous and asynchronous collaboration.
- Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status.
About US:
At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do.
Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.
This advertiser has chosen not to accept applicants from your region.
1
Medical Coder
Chennai, Tamil Nadu
UnitedHealth Group
Posted today
Job Viewed
Job Description
Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find a culture guided by inclusion, talented peers, comprehensive benefits and career development opportunities. Come make an impact on the communities we serve as you help us advance health optimization on a global scale. Join us to start **Caring. Connecting. Growing together.**
**Primary Responsibilities:**
+ Verifies and abstracts all the relevant data from the medical records to assign appropriate codes for the following settings: Multispecialty Outpatient Clinics, Urgent Care Centres, Inpatient Hospital Setting
+ Ability to code 12 charts per hour and meeting the standards for quality criteria
+ Needs to constantly track and implement all the updates of AMA guidelines, AHA guidelines, and CMS guidelines
+ Expertise in determining the EM levels ) based on MDM and appending modifiers to CPT codes as per NCCI edits and CPT guidelines
+ Ability to review and analyse medical records and add/modify CPT codes for minor surgical procedures, vaccines, and laboratory CPT codes as per documentation
+ Ability to extract and code various screening CPT codes and PQRS codes from the documentation
+ Ability to check NCCI edits and LCD & NCD coverage determinations and modify ICD-10-CM codes, CPT codes, and modifiers accordingly
+ An ideal team player who can work in a large group and provide inputs to the team for betterment of the team in terms of quality and productivity
+ Under general supervision, organizes and prioritizes all work to ensure that records are coded and edits are resolved in a timeframe that will assure compliance with regulatory and client guidelines
+ Adherence with confidentiality and maintains security of systems. Compliance with HIPAA policies and procedures for confidentiality of all patient records
+ Demonstrates knowledge of security of systems and associated policies and procedures for maintaining the security of the data contained within the systems
+ Comply with the terms and conditions of the employment contract, company policies and procedures, and any and all directives (such as, but not limited to, transfer and/or re-assignment to different work locations, change in teams and/or work shifts, policies in regard to flexibility of work benefits and/or work environment, alternative work arrangements, and other decisions that may arise due to the changing business environment). The Company may adopt, vary or rescind these policies and directives in its absolute discretion and without any limitation (implied or otherwise) on its ability to do so
**Required Qualifications:**
+ Experience: 1+ years in multispecialty Evaluation & Management medical coding.
+ Life Science or Allied Medicine Graduates with certification from AAPC or AHIMA.
+ Hands-on experience in coding multispecialty Evaluation & Management services such as Internal Medicine, Family Medicine, Urgent Care, Dermatology, Gastroenterology, Cardiology, Otolaryngology, etc.
+ Sound knowledge in Medical Terminology, Human Anatomy & Physiology
+ Proficient in ICD-10-CM, CPT, and HCPCS guidelines
_At UnitedHealth Group, our mission is to help people live healthier lives and make the health system work better for everyone. We believe everyone - of every race, gender, sexuality, age, location and income - deserves the opportunity to live their healthiest life. Today, however, there are still far too many barriers to good health which are disproportionately experienced by people of color, historically marginalized groups and those with lower incomes. We are committed to mitigating our impact on the environment and enabling and delivering equitable care that addresses health disparities and improves health outcomes - an enterprise priority reflected in our mission._
**Primary Responsibilities:**
+ Verifies and abstracts all the relevant data from the medical records to assign appropriate codes for the following settings: Multispecialty Outpatient Clinics, Urgent Care Centres, Inpatient Hospital Setting
+ Ability to code 12 charts per hour and meeting the standards for quality criteria
+ Needs to constantly track and implement all the updates of AMA guidelines, AHA guidelines, and CMS guidelines
+ Expertise in determining the EM levels ) based on MDM and appending modifiers to CPT codes as per NCCI edits and CPT guidelines
+ Ability to review and analyse medical records and add/modify CPT codes for minor surgical procedures, vaccines, and laboratory CPT codes as per documentation
+ Ability to extract and code various screening CPT codes and PQRS codes from the documentation
+ Ability to check NCCI edits and LCD & NCD coverage determinations and modify ICD-10-CM codes, CPT codes, and modifiers accordingly
+ An ideal team player who can work in a large group and provide inputs to the team for betterment of the team in terms of quality and productivity
+ Under general supervision, organizes and prioritizes all work to ensure that records are coded and edits are resolved in a timeframe that will assure compliance with regulatory and client guidelines
+ Adherence with confidentiality and maintains security of systems. Compliance with HIPAA policies and procedures for confidentiality of all patient records
+ Demonstrates knowledge of security of systems and associated policies and procedures for maintaining the security of the data contained within the systems
+ Comply with the terms and conditions of the employment contract, company policies and procedures, and any and all directives (such as, but not limited to, transfer and/or re-assignment to different work locations, change in teams and/or work shifts, policies in regard to flexibility of work benefits and/or work environment, alternative work arrangements, and other decisions that may arise due to the changing business environment). The Company may adopt, vary or rescind these policies and directives in its absolute discretion and without any limitation (implied or otherwise) on its ability to do so
**Required Qualifications:**
+ Experience: 1+ years in multispecialty Evaluation & Management medical coding.
+ Life Science or Allied Medicine Graduates with certification from AAPC or AHIMA.
+ Hands-on experience in coding multispecialty Evaluation & Management services such as Internal Medicine, Family Medicine, Urgent Care, Dermatology, Gastroenterology, Cardiology, Otolaryngology, etc.
+ Sound knowledge in Medical Terminology, Human Anatomy & Physiology
+ Proficient in ICD-10-CM, CPT, and HCPCS guidelines
_At UnitedHealth Group, our mission is to help people live healthier lives and make the health system work better for everyone. We believe everyone - of every race, gender, sexuality, age, location and income - deserves the opportunity to live their healthiest life. Today, however, there are still far too many barriers to good health which are disproportionately experienced by people of color, historically marginalized groups and those with lower incomes. We are committed to mitigating our impact on the environment and enabling and delivering equitable care that addresses health disparities and improves health outcomes - an enterprise priority reflected in our mission._
This advertiser has chosen not to accept applicants from your region.
2
Medical Advisor
Mumbai, Maharashtra
Abbott
Posted today
Job Viewed
Job Description
MAIN PURPOSE OF ROLE
Experienced professional individual contributor that works under limited supervision.
Applies subject matter knowledge in the area of Medical Affairs.
Requires capacity to apply skills/knowledge within the context of specific needs or requirements.
MAIN RESPONSIBILITIES
- As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills
in overseeing the direction, planning, execution, clinical trials/research and the data collection
activities.
- Contributes to implementation of clinical protocols, and facilitates completion of final reports.
- Recruits clinical investigators and negotiates study design and costs.
- Responsible for directing human clinical trials, phases III & IV for company products under
development.
- Participates in adverse event reporting and safety responsibilities monitoring.
- Coordinates and provides reporting information for reports submitted to the regulatory agencies.
- Monitors adherence to protocols and determines study completion.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
Experienced professional individual contributor that works under limited supervision.
Applies subject matter knowledge in the area of Medical Affairs.
Requires capacity to apply skills/knowledge within the context of specific needs or requirements.
MAIN RESPONSIBILITIES
- As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills
in overseeing the direction, planning, execution, clinical trials/research and the data collection
activities.
- Contributes to implementation of clinical protocols, and facilitates completion of final reports.
- Recruits clinical investigators and negotiates study design and costs.
- Responsible for directing human clinical trials, phases III & IV for company products under
development.
- Participates in adverse event reporting and safety responsibilities monitoring.
- Coordinates and provides reporting information for reports submitted to the regulatory agencies.
- Monitors adherence to protocols and determines study completion.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
This advertiser has chosen not to accept applicants from your region.
3
Medical Manager
Mumbai, Maharashtra
Sanofi Group
Posted 1 day ago
Job Viewed
Job Description
_1. Our position_
**_Job Title:_** _Medical Manager- Rare Blood Disorder_
**_Division / Business Unit: SE Asia & India MCO Medical, Pharma_**
**_Location:_** _Delhi/Mumbai_
**_Level:_** _L2-2_
**_Reporting to_** _: Rare Disease Medical Lead- SEA-I_
_2. About the job_
**Our Team:**
The SE Asia & India /Pharma Medical Team at Sanofi is a high-performing team of Medical leaders who are a trusted source of scientific and Medical information and shared insights; effective and innovative strategic partners to our internal and external stakeholders; and dedicated to public health. We represent diverse experiences and backgrounds which strengthens our team and mirrors the healthcare communities we engage.
**Main Responsibilities:**
Medical Advisor, Rare Blood Disorder will participate to and execute the Medical and scientific (non-promotional) strategy for the SE Asia & India MCO portfolio/ therapeutic area of Rare Blood Disroder in close partnership with the other functional franchise colleagues and in alignment with the overall franchise strategy.
The main responsibilities include:
**Strategy**
· The individual hired into this role must be strategic, solution-oriented, operationally savvy, creative, highly organized, flexible, able to build relationships and adept at handling multiple stakeholders.
**Responsibilities:**
+ Be the trusted scientific partner to key external experts by conducting timely, appropriate and frequent scientific exchanges to enhance the understanding of the scientific and medical value of our products.
+ Execute on stakeholder engagement plans to gather data, develop and share medical insights that contribute to the enhancement of Sanofi's key medical messages, and plans future research.
+ Keep abreast of medical and scientific developments in the therapeutic field to help identify and critically assess research opportunities and to play a supportive role in the execution of evidence generation plans to enhance the value of our products in a real-world setting.
+ Maintain effective and appropriate communication among internal stakeholders (Medical Affairs colleagues, Medical Information and Commercial Operations) while maintaining full compliance with relevant company, industry, legal and regulatory requirements;
+ Engage external stakeholders on medical and scientific information exchange for the therapeutic area during one-on-one interactions and group settings, exhibiting excellent scientific and clinical knowledge.
+ Use strong knowledge of relevant diseases and disease management protocols, healthcare environment and competitors to articulate the medical and scientific value of our products with external experts.
+ Establish robust, long-term peer relationships with Key Opinion Leaders and other Stakeholder partners.
+ Collaborate with Sanofi`s Diagnostic coordinator for the smooth operations of the companion diagnostic program.
+ Assimilate monthly country wise budget spends for the Medical activities, travel, diagnostic program and maintain a tracker for the same.
+ Effectively utilize the Scientific Engagement Model for attending and establishing a Sanofi Medical presence at relevant scientific congresses, symposia as directed.
+ Organizes educational meetings or local scientific advisory boards when requested.
+ Record/report insights and information appropriately, using available mechanisms and tools.
+ Collaborate, as directed, with Commercial Operations, Business Development, Regulatory, etc. to facilitate diligence reviews, medical and safety evaluation, product positioning, lifecycle evidence planning, and compliance needs.
+ Supports evidence-generation activities by aiding in data acquisition and identifying opportunities for further data collection clinical or investigator-led.
+ Responds to unsolicited requests regarding interest in Investigator-Sponsored Studies (ISS), and supports ISS submissions through appropriate internal processes.
**People Leadership:**
+ Drive strong collaborative relationships with commercial and cross-functional teams, including marketing, value & access, health economics, regulatory and clinical
+ Demonstrate strong leadership influencing across networks and by coaching and mentoring members of the team.
**External Stakeholder Engagement:**
+ Develop and implement stakeholder engagement strategy for Rare Blood Disorder products; and pipeline molecules to gain strategic insights in preparation for future launches
+ Develop and lead collaborations/ partnership with key professional societies and key experts.
+ Cultivate and maintain relationships with external experts.
+ Provide guidance on Rare Blood Disorder products and related medical issues and seek impactful insights
+ Provide scientific education on disease states, epidemiology, and clinical trials of Rare Blood Disorder products when relevant
+ Lead external advisory boards focused on Rare Blood Disorder products and pipeline
+ Provides high-quality, accurate, balanced and directed information to key customers and stakeholders in response to unsolicited requests for information, supports investigators in IIR submissions, management of Managed Access Program (MAP).
**Data Generation:**
+ Lead and drive rapid integrated evidence planning and execution through deep understanding of internal and external stakeholder evidence needs and robust data gaps analysis.
+ Work with relevant functions to coordinate the local and global approval process of new study proposals.
**Medical Operations:**
+ Review and /or approve promotional and non-promotional materials in accordance with internal procedures
+ Provide medical guidance and scientific education to internal stakeholders.
+ Ensure medical activities are executed according to franchise budget and cost-effective approaches are used to achieve strategic objectives
+ Ensure medical compliance in alignment with global policies and ensure medical activities are implemented with respect of the highest ethical standards.
**Context of the Job/ Major Challenges**
+ Guide the MSLs in their day-to-day activities and in collaboration with Rare Blood Disorder Medical Lead
+ Travel: 10 days per month Nationally and sometimes internationally.
+ Effectively mediate KOL's complex and controversial opinions vs; corporate policy decisions ensuring KOL relationships/medical strategy is not negatively impacted.
+ Ensures regulatory boundaries are non-promotional activities are respected vis-à-vis commercial partners.
**Scope of Role/Output**
+ Plan day-to-day interactions, including discussion points in accordance with the Medical Affairs strategy, establishing a frequency of interactions per stakeholder per year to ensure that objectives are met.
+ Executes on defined KOL territory strategy that is targeted to address diverse stakeholder needs (payers, patients, KOLs, HCP, etc.) and is aligned with company objectives.
+ Develops relevant medical strategy and guides cross functional
+ Uses approved scientific data during KOL interactions to advance the understanding of the therapeutic area.
_3. About you_
**Qualifications:**
+ Doctoral degree in a scientific discipline (M.D Pharmacology/ MBBS).
+ At least 4-5 Years of experience in the required area.
+ Experience in pharmaceutical industry, regulatory environment, clinical or preclinical research, and knowledge of a therapeutic area disease state and treatment.
+ Experience with basic research, drug discovery, drug development and SEE interactions.
+ Experience/knowledge of hematology/Hemophilia strongly preferred.
+ Strategic thinking and flawless execution with proven ability to prioritize deliverables and balance risk.
+ Strong analytical skills and affinity for problem solving.
+ Fluency in MS Office including Excel, word and powerpoint.
+ Exhibits integrity/trust
**Skills/Knowledge**
+ Actively listens to others and is adept at confidently stating expert opinion while respecting the positions of others
+ Utilizes effective, professional communications to cultivate strong working relationships with internal and external colleagues, flexible in own approach to people and situations.
+ Skillfully plans, prioritizes, and executes multiple responsibilities and projects. Demonstrates effective leadership skills (by example and through accomplishments), steps forward to handle challenges within scope of authority.
+ Deep understanding and knowledge of local regulations and codes of practice for the pharmaceutical industry, as they apply to the non-promotional activities of this role.
_Pursue progress, discover extraordinary_
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
All in for Diversity, Equity and Inclusion at Sanofi - YouTube (
**_Job Title:_** _Medical Manager- Rare Blood Disorder_
**_Division / Business Unit: SE Asia & India MCO Medical, Pharma_**
**_Location:_** _Delhi/Mumbai_
**_Level:_** _L2-2_
**_Reporting to_** _: Rare Disease Medical Lead- SEA-I_
_2. About the job_
**Our Team:**
The SE Asia & India /Pharma Medical Team at Sanofi is a high-performing team of Medical leaders who are a trusted source of scientific and Medical information and shared insights; effective and innovative strategic partners to our internal and external stakeholders; and dedicated to public health. We represent diverse experiences and backgrounds which strengthens our team and mirrors the healthcare communities we engage.
**Main Responsibilities:**
Medical Advisor, Rare Blood Disorder will participate to and execute the Medical and scientific (non-promotional) strategy for the SE Asia & India MCO portfolio/ therapeutic area of Rare Blood Disroder in close partnership with the other functional franchise colleagues and in alignment with the overall franchise strategy.
The main responsibilities include:
**Strategy**
· The individual hired into this role must be strategic, solution-oriented, operationally savvy, creative, highly organized, flexible, able to build relationships and adept at handling multiple stakeholders.
**Responsibilities:**
+ Be the trusted scientific partner to key external experts by conducting timely, appropriate and frequent scientific exchanges to enhance the understanding of the scientific and medical value of our products.
+ Execute on stakeholder engagement plans to gather data, develop and share medical insights that contribute to the enhancement of Sanofi's key medical messages, and plans future research.
+ Keep abreast of medical and scientific developments in the therapeutic field to help identify and critically assess research opportunities and to play a supportive role in the execution of evidence generation plans to enhance the value of our products in a real-world setting.
+ Maintain effective and appropriate communication among internal stakeholders (Medical Affairs colleagues, Medical Information and Commercial Operations) while maintaining full compliance with relevant company, industry, legal and regulatory requirements;
+ Engage external stakeholders on medical and scientific information exchange for the therapeutic area during one-on-one interactions and group settings, exhibiting excellent scientific and clinical knowledge.
+ Use strong knowledge of relevant diseases and disease management protocols, healthcare environment and competitors to articulate the medical and scientific value of our products with external experts.
+ Establish robust, long-term peer relationships with Key Opinion Leaders and other Stakeholder partners.
+ Collaborate with Sanofi`s Diagnostic coordinator for the smooth operations of the companion diagnostic program.
+ Assimilate monthly country wise budget spends for the Medical activities, travel, diagnostic program and maintain a tracker for the same.
+ Effectively utilize the Scientific Engagement Model for attending and establishing a Sanofi Medical presence at relevant scientific congresses, symposia as directed.
+ Organizes educational meetings or local scientific advisory boards when requested.
+ Record/report insights and information appropriately, using available mechanisms and tools.
+ Collaborate, as directed, with Commercial Operations, Business Development, Regulatory, etc. to facilitate diligence reviews, medical and safety evaluation, product positioning, lifecycle evidence planning, and compliance needs.
+ Supports evidence-generation activities by aiding in data acquisition and identifying opportunities for further data collection clinical or investigator-led.
+ Responds to unsolicited requests regarding interest in Investigator-Sponsored Studies (ISS), and supports ISS submissions through appropriate internal processes.
**People Leadership:**
+ Drive strong collaborative relationships with commercial and cross-functional teams, including marketing, value & access, health economics, regulatory and clinical
+ Demonstrate strong leadership influencing across networks and by coaching and mentoring members of the team.
**External Stakeholder Engagement:**
+ Develop and implement stakeholder engagement strategy for Rare Blood Disorder products; and pipeline molecules to gain strategic insights in preparation for future launches
+ Develop and lead collaborations/ partnership with key professional societies and key experts.
+ Cultivate and maintain relationships with external experts.
+ Provide guidance on Rare Blood Disorder products and related medical issues and seek impactful insights
+ Provide scientific education on disease states, epidemiology, and clinical trials of Rare Blood Disorder products when relevant
+ Lead external advisory boards focused on Rare Blood Disorder products and pipeline
+ Provides high-quality, accurate, balanced and directed information to key customers and stakeholders in response to unsolicited requests for information, supports investigators in IIR submissions, management of Managed Access Program (MAP).
**Data Generation:**
+ Lead and drive rapid integrated evidence planning and execution through deep understanding of internal and external stakeholder evidence needs and robust data gaps analysis.
+ Work with relevant functions to coordinate the local and global approval process of new study proposals.
**Medical Operations:**
+ Review and /or approve promotional and non-promotional materials in accordance with internal procedures
+ Provide medical guidance and scientific education to internal stakeholders.
+ Ensure medical activities are executed according to franchise budget and cost-effective approaches are used to achieve strategic objectives
+ Ensure medical compliance in alignment with global policies and ensure medical activities are implemented with respect of the highest ethical standards.
**Context of the Job/ Major Challenges**
+ Guide the MSLs in their day-to-day activities and in collaboration with Rare Blood Disorder Medical Lead
+ Travel: 10 days per month Nationally and sometimes internationally.
+ Effectively mediate KOL's complex and controversial opinions vs; corporate policy decisions ensuring KOL relationships/medical strategy is not negatively impacted.
+ Ensures regulatory boundaries are non-promotional activities are respected vis-à-vis commercial partners.
**Scope of Role/Output**
+ Plan day-to-day interactions, including discussion points in accordance with the Medical Affairs strategy, establishing a frequency of interactions per stakeholder per year to ensure that objectives are met.
+ Executes on defined KOL territory strategy that is targeted to address diverse stakeholder needs (payers, patients, KOLs, HCP, etc.) and is aligned with company objectives.
+ Develops relevant medical strategy and guides cross functional
+ Uses approved scientific data during KOL interactions to advance the understanding of the therapeutic area.
_3. About you_
**Qualifications:**
+ Doctoral degree in a scientific discipline (M.D Pharmacology/ MBBS).
+ At least 4-5 Years of experience in the required area.
+ Experience in pharmaceutical industry, regulatory environment, clinical or preclinical research, and knowledge of a therapeutic area disease state and treatment.
+ Experience with basic research, drug discovery, drug development and SEE interactions.
+ Experience/knowledge of hematology/Hemophilia strongly preferred.
+ Strategic thinking and flawless execution with proven ability to prioritize deliverables and balance risk.
+ Strong analytical skills and affinity for problem solving.
+ Fluency in MS Office including Excel, word and powerpoint.
+ Exhibits integrity/trust
**Skills/Knowledge**
+ Actively listens to others and is adept at confidently stating expert opinion while respecting the positions of others
+ Utilizes effective, professional communications to cultivate strong working relationships with internal and external colleagues, flexible in own approach to people and situations.
+ Skillfully plans, prioritizes, and executes multiple responsibilities and projects. Demonstrates effective leadership skills (by example and through accomplishments), steps forward to handle challenges within scope of authority.
+ Deep understanding and knowledge of local regulations and codes of practice for the pharmaceutical industry, as they apply to the non-promotional activities of this role.
_Pursue progress, discover extraordinary_
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( **_progress_** **, discover** **_extraordinary_**
Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video ( and check out our Diversity Equity and Inclusion actions at sanofi.com ( !
Global Terms & Conditions and Data Privacy Statement ( is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting or via our movie We are Sanofi ( an organization, we change the practice of medicine; reinvent the way we work; and enable people to be their best versions in career and life. We are constantly moving and growing, making sure our people grow with us. Our working environment helps us build a dynamic and inclusive workplace operating on trust and respect and allows employees to live the life they want to live.
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4
Medical Advisor
Sun Pharmaceuticals, Inc
Posted 2 days ago
Job Viewed
Job Description
**Job Title:**
Medical Advisor
**Business Unit:**
Medical Services
**Location :**
Mumbai
At Sun Pharma, we commit to helping you **Create your own sunshine** by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
**Are You Ready to Create Your Own Sunshine?**
As you enter the Sun Pharma world, youll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each others journeys.
**Key responsibilities:**
+ Core scientific member of cross-functional franchise team and a disease area expert, responsible for scientific enablement of respective business cluster
+ Conceptualization and project management of wide range of medical activities that are aligned to the respective franchise strategy like:
+ New Product Ideation
+ New Product Evaluation
+ Therapeutic rationale & relevant Medical support for regulatory submissions
+ Preparation of SEC presentations & defense in SEC meeting
+ Pre-launch & launch preparations including product monograph, training manuals, training & CME slides
+ Franchise Medical Education programs
+ Promotional and non-promotional material review & approval
+ Answering queries
+ Marketing and Sales training
+ Real World Clinical Research and Publications Planning and Execution
+ Advisory board meetings
+ Developing Insight driven Medical Plans
+ Interaction & Engagement of identified Key Opinion leaders in a peer-to-peer capacity through medical affairs activities, in alignment with the overall strategic plan to shape disease areas of interest
+ A therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, obtain insights into patients treatment trends and insights in the disease areas of interest and to be considered a trusted scientific counterpart
+ Responsible for identifying knowledge gaps, practice gaps and data gaps and provide recommendations for devising medical & product education programs, evidence generation and special projects
+ Ability to convert insights on disease trends and treatment patterns from KOLs into viable and formidable solutions to shape the therapeutic areas of interest
+ Devise optimal training plan to ensure flow of latest medical developments in the given to sales & marketing team
+ Jointly responsible with marketing teams to support optimal patient outcomes through communication of data, information, and insights to shape disease areas of interest
+ Represent the organization in various internal & external scientific platforms
+ Collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in journals of repute
+ Receiving and processing scientific information requests received from physicians & internal stakeholders
+ Ability to handle complex questions from health care professionals related to company products or disease area to satisfaction
+ Responsible for ensuring that all promotional materials are approved within stipulated timelines and in alignment with company approval process
+ Conduct of robust medical evaluation of new products through thorough desk research and interactions with KOLs
**Travel Estimate**
Less than 1 week in a month
**Job Requirements**
**Educational Qualification**
MD Pharmacology
**Experience**
1-3 years working experience in the pharmaceutical industry or research company in a capacity of HO Medical Advisor or Sr. Medical Advisor
+ Training in medical writing, clinical trial methodologies, research design and ICH GCP will be added advantage
+ Must have working knowledge of Indian regulations pertaining to Health care professionals interactions (MCI code of ethics for doctors & UCPMP Code for Pharma) and Drugs and Cosmetic Act regulations pertaining to clinical trials and new drug approvals
+ Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data
+ Strategic mindset with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer capacity
+ Experience with complex business environments preferred
+ Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and award
**Your Success Matters to Us**
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. _Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Lets create a brighter future together!_
**_Disclaimer:_** _The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s)._
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
Medical Advisor
**Business Unit:**
Medical Services
**Location :**
Mumbai
At Sun Pharma, we commit to helping you **Create your own sunshine** by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
**Are You Ready to Create Your Own Sunshine?**
As you enter the Sun Pharma world, youll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each others journeys.
**Key responsibilities:**
+ Core scientific member of cross-functional franchise team and a disease area expert, responsible for scientific enablement of respective business cluster
+ Conceptualization and project management of wide range of medical activities that are aligned to the respective franchise strategy like:
+ New Product Ideation
+ New Product Evaluation
+ Therapeutic rationale & relevant Medical support for regulatory submissions
+ Preparation of SEC presentations & defense in SEC meeting
+ Pre-launch & launch preparations including product monograph, training manuals, training & CME slides
+ Franchise Medical Education programs
+ Promotional and non-promotional material review & approval
+ Answering queries
+ Marketing and Sales training
+ Real World Clinical Research and Publications Planning and Execution
+ Advisory board meetings
+ Developing Insight driven Medical Plans
+ Interaction & Engagement of identified Key Opinion leaders in a peer-to-peer capacity through medical affairs activities, in alignment with the overall strategic plan to shape disease areas of interest
+ A therapeutic area scientific expert, responsible for discussing the scientific data pertaining to products on proactive and reactive basis, obtain insights into patients treatment trends and insights in the disease areas of interest and to be considered a trusted scientific counterpart
+ Responsible for identifying knowledge gaps, practice gaps and data gaps and provide recommendations for devising medical & product education programs, evidence generation and special projects
+ Ability to convert insights on disease trends and treatment patterns from KOLs into viable and formidable solutions to shape the therapeutic areas of interest
+ Devise optimal training plan to ensure flow of latest medical developments in the given to sales & marketing team
+ Jointly responsible with marketing teams to support optimal patient outcomes through communication of data, information, and insights to shape disease areas of interest
+ Represent the organization in various internal & external scientific platforms
+ Collaborate with thought leaders to conduct therapy specific reviews, meta-analysis, case studies, case series, patient reported outcomes and publish them in journals of repute
+ Receiving and processing scientific information requests received from physicians & internal stakeholders
+ Ability to handle complex questions from health care professionals related to company products or disease area to satisfaction
+ Responsible for ensuring that all promotional materials are approved within stipulated timelines and in alignment with company approval process
+ Conduct of robust medical evaluation of new products through thorough desk research and interactions with KOLs
**Travel Estimate**
Less than 1 week in a month
**Job Requirements**
**Educational Qualification**
MD Pharmacology
**Experience**
1-3 years working experience in the pharmaceutical industry or research company in a capacity of HO Medical Advisor or Sr. Medical Advisor
+ Training in medical writing, clinical trial methodologies, research design and ICH GCP will be added advantage
+ Must have working knowledge of Indian regulations pertaining to Health care professionals interactions (MCI code of ethics for doctors & UCPMP Code for Pharma) and Drugs and Cosmetic Act regulations pertaining to clinical trials and new drug approvals
+ Strong academic record with deep knowledge of the therapeutic area, strength in research with knowledge of research methodologies and interpretation of medical data
+ Strategic mindset with scientific acumen and communication skills in order to be accepted by leading specialists in peer-to-peer capacity
+ Experience with complex business environments preferred
+ Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and award
**Your Success Matters to Us**
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. _Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Lets create a brighter future together!_
**_Disclaimer:_** _The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s)._
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
This advertiser has chosen not to accept applicants from your region.
5
Medical Transcriptionist
HighPoints Technologies India (P) Ltd
Posted today
Job Viewed
Job Description
Role Overview
We are looking to hire experienced Sr. Medical Transcriptionists / Editors who can accurately transcribe and edit radiology and diagnostic reports, while maintaining the highest standards of quality, compliance, and medical accuracy.
Key Responsibilities
- Transcribe radiology reports with high accuracy and adherence to medical standards
- Edit and format transcriptions for clarity, consistency, and compliance
- Coordinate with radiologists to resolve unclear or incomplete inputs
- Maintain strict confidentiality in handling patient medical information
- Stay current with industry best practices and evolving documentation guidelines
Qualifications & Skills
Education & Typing:
- B.Sc. in Science
- Typing speed of at least 40 WPM
Skills Required:
- Proficiency in transcription and editing tools
- Excellent English communication – both written and verbal
- Strong attention to detail and accuracy
- Familiarity with medical terminology and diagnostic procedures
- Strong time management and deadline orientation
- Commitment to confidentiality and healthcare compliance
Ideal Candidate
- Has 3–6 years’ experience in medical transcription/editing, especially in radiology
- Stays near the office
- Comfortable working in rotational shifts
- Can work independently and as part of a team
This advertiser has chosen not to accept applicants from your region.
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About the latest Medical internship Jobs in India !
6
Medical Scribe
Triple
Posted today
Job Viewed
Job Description
Triple
Triple is leading the way in remote work solutions, helping small and medium-sized businesses in North America build highly efficient remote teams for Administration, Customer Service, Accounting, Operations, and back-office roles. Our focus has always been on our Clients, People, and Planet, ensuring our operations contribute positively across these key areas. Distinguished by its rigorous standards, Triple excels in:
- Selectively recruiting the top 1% of industry professionals
- Delivering in-depth training to ensure peak performance
- Offering superior account management for seamless operations
Embrace unparalleled professionalism and efficiency with Triple—where we redefine the essence of remote hiring.
Summary
We are looking for an enthusiastic, detail-oriented, experienced, and knowledgeable medical scribe to assist our client’s healthcare team with documenting patient medical records. The successful applicant will be responsible for documenting accurate and detailed information on patient visits. The ideal candidate will adhere to practice protocols and processes, and effectively manage the volume of work without allowing quality to be compromised. If you have prior experience working in a similar role, we encourage you to apply.
Responsibilities
- Prepare and assemble medical record documentation/charts for physicians.
- Scribe medical record documentation utilizing electronic medical record applications.
- Ensure medical record compliance by self-documentation attestation.
- Update patient history, physical exam, and other pertinent health information in the prescribed format.
- Prepare and send all documentation to physicians for review and approval via authentication of detailed data entry and facility-specific procedures.
- Complies with hospital and medical facility policies, including those relating to HIPAA.
- Performs other clerical duties and tasks to improve provider productivity and clinic workflow as assigned.
Qualifications/Skills
- Bachelor’s/Master’s degree in a related domain
- Minimum 3 years of work experience in a similar domain
- Experience with US-based clinics/hospitals is a must
- Experience with internal medicine
- Familiarity with medical terminology & medical summarization
- Excellent English professional writing skills; including advanced proficiency in grammar and spelling.
- Ability to work independently in a secure and private location with a reliable high-speed internet connection.
- Ability to participate in live audio/video chats and screen-sharing sessions.
Schedule (US Shifts Only)
Eastern Time - 5:30 p.m. - 2:30 a.m. IST, Rotational Shifts
Pacific Time - 9:30 p.m. - 6:30 a.m. IST, Rotational Shifts
Logistical Requirements
Quiet and brightly illuminated work environment
Laptop with Minimum 8GB RAM, I5 8th gen processor
720P Webcam and Headset
A reliable ISP with a minimum speed of 100 Mbps
Smartphone
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7
Medical Writer
72 Dragons
Posted 5 days ago
Job Viewed
Job Description
We are looking for a Health Professional (Medicine, biotechnology, pharmacy, nursing, microbiology, dentistry, or biomedical sciences), to join our health writing team. This is a full-time position in India. The candidate must have a health and science background and experience writing in-depth medical content. The writer will be responsible for creating the content for the 72 Dragons Health channel, including articles and digital media posts.
About the Company:
- 72 Dragons is a global company that caters to multiple sectors. There are 3 sectors in our company: Art, Film, and Health. This position will focus mostly on Health, targeting healthcare professionals.
- 72 Dragons provides social media and film production services to the health industry and professionals, including medical doctors and other healthcare professionals, as well as institutions or companies such as hospitals, pharmaceuticals, medical institutes, international agencies, and community organizations.
Job Responsibilities include, but are not limited to:
- Write in-depth articles on medical topics The target audience is healthcare professionals worldwide.
- Establish the tone of voice for the 72 Dragons Health Channel. The content is cutting-edge, featuring the latest medical news and trending medical topics worldwide. It also has strong links to the film and art worlds, which makes 72 Dragons stand out from other companies.
- Work with the social media and digital marketing team to strategize on creating content that reaches our target audience.
- Collaborative work with the Health Writing team, Visual Media, and Curation Writers team.
- Ensuring relevant and top pieces of information are delivered through all our digital channels that reach our target audience: Facebook, Instagram, YouTube, 72 Dragons Health Website
- Ensure that safe working practices and protocols are followed while publishing on digital media, such as plagiarism checks and image credits. The content MUST be original.
- Academic research on health and related fields
Requirements
- A graduate with a health and science degree
- A strong knowledge of the various medical fields, medical terminology, and academic research.
- Excellent spoken and written English Skills.
- Ability to think creatively and come up with innovative ideas for content creation.
- Basic knowledge of Canva, Google Docs, Google Slides, Google Sheets, and Gmail is required.
- Exposure to reference & citation management tools, preferably Zotero.
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8
Medical Doctor
Pune, Maharashtra
ALIV - Regenerative Wellness
Posted 5 days ago
Job Viewed
Job Description
Location: Pune, India
Experience: 3–7 years
Employment Type: Full-time
ALIV is India’s pioneer in regenerative wellness and IV infusion therapies, offering personalized protocols that combine medical precision with holistic care. Our clinics are designed to deliver premium patient experiences while setting the standard for safe, ethical, and cutting-edge therapies across the country.
We are looking for qualified doctors (BHMS, BAMS, MBBS) to join our Mumbai clinical team as Medical Counselors and Clinical Support Doctors . This hybrid role combines patient consultation, IV infusion oversight, emergency preparedness, and surgical assistance experience .
The ideal candidate will excel in both patient-facing counseling and hands-on clinical skills — particularly IV line setup, infusion therapy administration, and minor procedure assistance — while providing empathetic guidance to patients about their treatments.
- Conduct detailed consultations, review medical histories, and ensure accurate EMR documentation.
- Educate and counsel patients on IV protocols, regenerative therapies, and treatment plans in clear, empathetic language.
- Address patient queries, building trust and confidence before, during, and after treatments.
- Flawlessly set up IV lines — ensuring one-prick, pain-free insertion for every patient.
- Oversee IV infusions and regenerative therapy administration in compliance with ALIV protocols.
- Support physicians in minor procedures, regenerative injectables, and surgical preparation when needed.
- Monitor patient vitals, identify early warning signs, and act quickly in emergencies.
- Ensure patients are well-prepared for procedures, with complete pre-treatment clearances and education.
- Provide post-infusion guidance, including hydration, medication, and activity instructions.
- Follow up on recovery progress and ensure seamless patient handover for continuing care.
- Work closely with nurses, therapists, and front desk staff to ensure smooth patient journeys.
- Participate in skill-upgrading sessions, mock drills, and ongoing training to maintain top-tier clinical performance.
- BHMS, BAMS, or MBBS degree with valid registration under the relevant council (MCI/State Council).
- 3–7 years of clinical experience , with:
- Proven hands-on expertise in IV cannulation (speed, accuracy, and patient comfort are key).
- Exposure to ICU/critical care environments and emergency management protocols.
- Experience assisting in surgical or procedural setups.
- Calm, steady-handed, and precision-focused — committed to pain-free patient care .
- Strong counseling skills, able to explain complex medical concepts simply and empathetically.
- Proactive, collaborative approach to working with multidisciplinary teams.
- Passion for wellness and regenerative medicine; eager to grow in a cutting-edge field.
- Opportunity to shape the future of preventative and regenerative care in India .
- Access to world-class training in IV infusion therapy and regenerative protocols.
- Competitive salary and performance-based incentives.
- A patient-first work culture with no night shifts and focus on quality over quantity.
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9