1,024 Medical Affairs jobs in India
Medical Affairs - Medical Writing
Posted today
Job Viewed
Job Description
- Medical Affairs - Medical Writing
- Position title/level may vary by site or geographic location
Purpose:
- Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across the entire drug development lifecycle is fundamental to Lilly.
- As healthcare providers are deluged with data and are making choices in an increasingly complex and stressed health system, Lilly Medical Affairs is able to provide clear, credible answers that will set Lilly apart from its competitors. Medical Affairs’ mission is to make Lilly the preferred pharmaceutical partner in the healthcare community globally by leveraging its medical expertise to drive patient-centric answers and solutions. Medical Affairs (MA) brings deep medical expertise to healthcare providers and payers. MA focuses on answering their questions with customized clinical and real-world evidence that can make the difference on if and how they use Lilly products. Additionally, MA brings clinical insights from customers back to the company to inform new product development and lifecycle planning. MA also supports patients with educational tools to help them manage their illness and with assistance to access our medicines for those facing tough financial situations. The MA content development team will be key in maintaining and creating content to support Medical Affairs activities such as:
- Slide Updates
- Internal Training Slides
- Manuscript Slides
- Data Slides
- Newsletters/ bulletin
- QR Compendium
- Affiliate Regional Slides
- HCP & patient education material
- Advisory board slides
- Competitive landscape slides
- Image sourcing, image redraws
- Lexicon
- MQAD (Medical Questions Analysis Document)
- Primary Responsibilities:
- This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.
EMS (Executive Medical Summary)
- Content Strategy and Execution: Document Preparation, Development and Finalization/Document Management- Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects.-
- Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review, coordinate, and complete the regulatory documents supporting clinical development/product registration.-
- Conduct effective document initiation meeting to ensure authoring team alignment and understanding.-
- Build scientific-based rationale that support the purpose of more complex and/or strategic documents.-
- Ensure data are presented in a clear, complete, accurate, and concise manner.-
- Ensure that key data, statements and conclusions are consistent across related documents, and that statements and conclusions are integrated, accurate, balanced and supported by appropriate data.-
- Coordinate expert/scientific reviews, collate reviewer’s comments, adjust content of document as required based on internal/external input, and prepare final version.-
- Ensure and coordinate quality checks for accuracy.-
- Exhibit flexibility in moving across development and preparation of multiple document types.-
- Influence or negotiate change of timelines and content with other team members.-
- Work with internal and external experts to develop and prepare presentations.-
- As needed, may build and manage relationships with vendors/alliance partners.Project and Stakeholder management- Build/communicate credible writing project timelines.-
- Anticipate and mitigate risks to delivery-
- Work with teams and stakeholders to ensure smooth and timely development of documents and escalate issues, as appropriate, to ensure document completion.-
- Effectively communicate project status to stakeholdersKnowledge and Skills Development- Maintain and enhance therapeutic area knowledge including disease state and compound(s) for assigned project(s).-
- Exhibit flexibility in moving across document types, therapeutic areas, an
Medical Affairs - Medical Writing
Posted today
Job Viewed
Job Description
**Purpose**:
Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across the entire drug development lifecycle is fundamental to Lilly.
As healthcare providers are deluged with data and are making choices in an increasingly complex and stressed health system, Lilly Medical Affairs is able to provide clear, credible answers that will set Lilly apart from its competitors. Medical Affairs’ mission is to make Lilly the preferred pharmaceutical partner in the healthcare community globally by leveraging its medical expertise to drive patient-centric answers and solutions. Medical Affairs (MA) brings deep medical expertise to healthcare providers and payers. MA focuses on answering their questions with customized clinical and real-world evidence that can make the difference on if and how they use Lilly products. Additionally, MA brings clinical insights from customers back to the company to inform new product development and lifecycle planning. MA also supports patients with educational tools to help them manage their illness and with assistance to access our medicines for those facing tough financial situations. The MA content development team will be key in maintaining and creating content to support Medical Affairs activities such as:
- Slide Updates
- Internal Training Slides
- Manuscript Slides
- Data Slides
- Newsletters/ bulletin
- QR Compendium
- Affiliate Regional Slides
- HCP & patient education material
- Advisory board slides
- Competitive landscape slides
- Image sourcing, image redraws
- Lexicon
- MQAD (Medical Questions Analysis Document)
**Primary Responsibilities**:
This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.
**EMS (Executive Medical Summary)**
Content Strategy and Execution: Document Preparation, Development and Finalization/Document Management
- Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects.
- Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review, coordinate, and complete the regulatory documents supporting clinical development/product registration.
- Conduct effective document initiation meeting to ensure authoring team alignment and understanding.
- Build scientific-based rationale that support the purpose of more complex and/or strategic documents.
- Ensure data are presented in a clear, complete, accurate, and concise manner.
- Ensure that key data, statements and conclusions are consistent across related documents, and that statements and conclusions are integrated, accurate, balanced and supported by appropriate data.
- Coordinate expert/scientific reviews, collate reviewer’s comments, adjust content of document as required based on internal/external input, and prepare final version.
- Ensure and coordinate quality checks for accuracy.
- Exhibit flexibility in moving across development and preparation of multiple document types.
- Influence or negotiate change of timelines and content with other team members.
- Work with internal and external experts to develop and prepare presentations.
- As needed, may build and manage relationships with vendors/alliance partners.
Project and Stakeholder management
- Build/communicate credible writing project timelines.
- Anticipate and mitigate risks to delivery
- Work with teams and stakeholders to ensure smooth and timely development of documents and escalate issues, as appropriate, to ensure document completion.
- Effectively communicate project status to stakeholders
Knowledge and Skills Development
- Maintain and enhance therapeutic area knowledge including disease state and compound(s) for assigned project(s).
- Exhibit flexibility in moving across document types, therapeutic areas, and compounds, depending on project assignment.
- Maintain and enhance knowledge of regulatory guidelines and pub
Medical Affairs Specialist
Posted today
Job Viewed
Job Description
- Developing and executing medical affairs strategies in alignment with brand objectives.
- Serving as a scientific expert for the company's product portfolio.
- Engaging with Key Opinion Leaders (KOLs) and healthcare professionals to discuss scientific and clinical data.
- Reviewing and approving promotional and non-promotional materials to ensure scientific accuracy and compliance.
- Developing scientific communication plans and materials, such as slide decks and FAQs.
- Supporting the planning and execution of medical education programs and symposia.
- Analyzing clinical trial data and literature to support medical strategies.
- Responding to unsolicited medical information requests from healthcare professionals.
- Collaborating with cross-functional teams, including R&D, marketing, and regulatory affairs.
- Ensuring adherence to all relevant industry codes and regulatory requirements.
- Advanced degree (Master's, Pharm.D., Ph.D.) in a life science, medical, or related field.
- Minimum of 3-5 years of experience in medical affairs, clinical development, or a related pharmaceutical role.
- In-depth knowledge of the pharmaceutical industry, therapeutic areas, and regulatory landscape.
- Excellent scientific communication and presentation skills.
- Strong analytical and critical thinking abilities.
- Proven ability to build and maintain relationships with medical experts.
- Proficiency in data analysis and interpretation.
- Understanding of ethical guidelines and compliance in medical communications.
- Ability to travel to medical conferences and engage with healthcare professionals.
Medical Affairs Manager
Posted today
Job Viewed
Job Description
About AstraZeneca
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies.
Roles & Responsibilities:
Office based medical leader who can be a single contributor as well as be responsible for a team within a given Therapy Area or for a significant product to ensure the company business unit goals are achieved. Accountable for strategic Therapy Area direction and scientific leadership within the Medical Affairs Team.
Embeds a deep healthcare system practices and gaps understanding (environment, priorities, clinical and patient pathways, etc) that can translate into actionable strategies within the local Medical Plans. Accountable for developing and execution of the Therapy Area/Product Medical Affairs Plans composed of confidence and evidence generation activities, as well as fundamental and sustainable clinical practice transformations that strengthen healthcare ecosystems, improve treatment outcomes, drive meaningful changes in patient care and treatment paradigms and enable access to quality care in alignment with the company’s portfolio. Recognizes and incorporates innovation wherever appropriate into Medical Affairs strategic plans and lead in execution to drive strategic and sustainable impact internally and externally to support the adoption of evidence-based practices, guidelines, and treatment approaches. Acts as a catalysts of sustainable healthcare ecosystem change, enhancing access to quality care for patients and enabling the adoption of our innovative medicines.
Ensures that all local medical requirements are met for all product/TA material and will use medical expertise to contribute to the marketing direction of the product/TA. Recognised as a medical expert within the local marketing company and be responsible for providing medical leadership, expertise, and strategic input to ensure that the Medical Affairs plans align with the broader business objectives. Collaborate with relevant cross-functional teams identify, activate and measure scalable healthcare practice shaping initiatives with integrated partnership engagement plans composed of key traditional ( HCPs) and non-traditional ( policy and decision makers, PAGs, government, innovative solution providers) stakeholders. Able to lead a significant cross functional, projects. For example, projects like RWE, pre-launch, post-launch clinical trials or market access projects. Works to ensure operational excellence and collaborates with compliance to ensure adherence to company standards.
Typical Accountabilities
Medical strategy and clinical input
Team & People Management:
Medical Governance Oversight
Education, Qualifications, Skills, and Experience
Essential
Desirable
Why AstraZeneca?
At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare.
You can find alternative messaging to use in the ‘Global Talent Attraction Story messaging’ section of the Global Playbook on the - try to use other examples in order to make it different for candidates!
So, what’s next?
Where can I find out more?
Our Social Media, Follow AstraZeneca on LinkedIn
Follow AstraZeneca on Facebook
Follow AstraZeneca on Instagram
If you have site, country or departmental social media then feel free to switch any of the above links.
Date Posted
02-Jul-2025Closing Date
14-Jul-2025Regulatory Affairs - Medical Devices
Posted today
Job Viewed
Job Description
Job Description
Role - Regulatory Affairs - Medical Devices
Experience - 1 to 3 Years
Location- Madhavaram, Chennai
Budget - As per the industry
Key Responsibilities:
1. Regulatory Submissions: Prepare and submit regulatory documents to authorities for approval, such as new product applications, amendments, and supplements.
2. Compliance: Ensure products meet regulatory requirements, including safety, efficacy, and quality standards.
3. Regulatory Intelligence: Stay up-to-date with changing regulations, guidelines, and industry standards.
4. Risk Management: Identify and mitigate risks associated with products or processes.
5. Collaboration: Work with cross-functional teams, including R&D, Quality, and Manufacturing.
6. Documentation: Maintain accurate and detailed records of regulatory activities, including submissions, approvals, and compliance.
Requirements:
1. Education: Bachelor's degree in a relevant field, such as life sciences, pharmacy, or engineering.
2. Experience: Prior experience in regulatory affairs, quality assurance, or a related field.
3. Knowledge: Strong understanding of regulatory requirements, guidelines, and industry standards.
4. Communication: Excellent written and verbal communication skills.
5. Analytical: Ability to analyze complex regulatory information and identify key issues.
Skills:
1. Regulatory writing: Ability to write clear, concise, and compliant regulatory documents.
2. Project management: Ability to manage multiple projects and prioritize tasks effectively.
3. Attention to detail: Strong attention to detail and ability to ensure accuracy and compliance.
4. Collaboration: Ability to work effectively with cross-functional teams and build strong relationships.
Certifications:
1. RAC (Regulatory Affairs Certification): A certification offered by the Regulatory Affairs Professionals Society (RAPS) that demonstrates expertise in regulatory affairs.
Overall, a Regulatory Affairs professional plays a critical role in ensuring compliance with regulatory requirements and facilitating the development and approval of products.
Regulatory Affairs - Medical Devices
Posted 15 days ago
Job Viewed
Job Description
Job Description
Role - Regulatory Affairs - Medical Devices
Experience - 1 to 3 Years
Location- Madhavaram, Chennai
Budget - As per the industry
Key Responsibilities:
1. Regulatory Submissions: Prepare and submit regulatory documents to authorities for approval, such as new product applications, amendments, and supplements.
2. Compliance: Ensure products meet regulatory requirements, including safety, efficacy, and quality standards.
3. Regulatory Intelligence: Stay up-to-date with changing regulations, guidelines, and industry standards.
4. Risk Management: Identify and mitigate risks associated with products or processes.
5. Collaboration: Work with cross-functional teams, including R&D, Quality, and Manufacturing.
6. Documentation: Maintain accurate and detailed records of regulatory activities, including submissions, approvals, and compliance.
Requirements:
1. Education: Bachelor's degree in a relevant field, such as life sciences, pharmacy, or engineering.
2. Experience: Prior experience in regulatory affairs, quality assurance, or a related field.
3. Knowledge: Strong understanding of regulatory requirements, guidelines, and industry standards.
4. Communication: Excellent written and verbal communication skills.
5. Analytical: Ability to analyze complex regulatory information and identify key issues.
Skills:
1. Regulatory writing: Ability to write clear, concise, and compliant regulatory documents.
2. Project management: Ability to manage multiple projects and prioritize tasks effectively.
3. Attention to detail: Strong attention to detail and ability to ensure accuracy and compliance.
4. Collaboration: Ability to work effectively with cross-functional teams and build strong relationships.
Certifications:
1. RAC (Regulatory Affairs Certification): A certification offered by the Regulatory Affairs Professionals Society (RAPS) that demonstrates expertise in regulatory affairs.
Overall, a Regulatory Affairs professional plays a critical role in ensuring compliance with regulatory requirements and facilitating the development and approval of products.
Regional Manager - Medical Affairs
Posted 2 days ago
Job Viewed
Job Description
+ **Designation:** Regional Manager - Medical Affairs
+ **Reporting** : Associate director, SMA
+ **Region to be covered** **: India- North and West**
+ **Location** **: West or North**
+ **Minimum Qualification & Experience:** **MD/MBBS/MDS/BDS with at least 3-5 years of experience in regional/ medico marketing role with a** **pharmaceutical/nutrition** **company.**
+ **Critical Skills Required:**
+ Possess excellent interpersonal, communication, coordination, and time-management skills.
+ Ability to problem solve, work in teams, lead others toward defined objectives and present complex data clearly are also critical.
+ Able to work independently and meticulously.
+ Adaptable and having the ability to work under a wide variety of conditions.
+ Able to prepare and make effective scientific presentations - These can include internal presentations for their own department, presentations for HCPs at different forums.
+ **Key Responsibilities:**
+ Travel to respective places and be the owner of all scientific activities in the assigned regions.
+ Active participation in scientific programs as speakers through lectures/presentations to propagate scientific communication to target audience.
+ Ownership and responsibility for conducting all head office driven HCP E-engagement platforms as decided by the division head.
+ Field work with regional sales teams (face to face calls or E-calls with HCPs as per feasibility and company policy).
+ **Facilitate the exchange of unbiased scientific information between the medical community and the company.**
+ **Liaison with key opinion leaders on educational and** **clinically/scientifically** **oriented initiatives to establish long-term collaborative relationships and advocacy.**
+ **Responsible for identifying, segmenting and developing KOLs in various therapeutic areas in terms of specialty, experience and academic interest.**
+ **Responsible for medical information services (MIS). Responsibilities include supporting sales force in providing information to physicians related to latest developments in medical research, current recommendations on Standard of Care across therapeutic areas and resolving queries.**
+ **Continuously update medical/ product knowledge of field force and training of recruit in the region in coordination with the training team.**
+ **Communicating at an ongoing basis** **competitive/scientific** **intelligence from region to medical director/medical affairs team to ensure timely objection handling/ scientific support to sale** **s marketing teams to handle competitor objections.**
+ **All activities to be carried out in accordance with policies laid down by the company. To ensure all the medical and promotional activities are run in a compliant manner as per the internal guidelines, country regulations and local industry codes of promotional practices.**
+ **Roles and responsibilities may change as per the requirement of the company as defined by division head.**
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
Be The First To Know
About the latest Medical affairs Jobs in India !
Senior Medical Affairs Manager
Posted 3 days ago
Job Viewed
Job Description
Medical Affairs Lead (IHS)
Posted today
Job Viewed
Job Description
About WhiteCrow
We are global talent research, insight and pipelining specialists with offices in the UK, USA, Singapore, Malaysia, Hong Kong, Dubai, and India. Our international reach has helped us to understand and penetrate specialist markets at a global level. In addition to this, our service is also extended to complement our client's in-house research.
About our client
Our client is a a Singapore based, healthcare multi-national company with operations in SEA, Middle East and North Africa with established plan for global expansion. Their main focus is on sales, marketing and distribution of Pharmaceutical, Medical Devices, Diagnostics & OTC products. They aim to serve clients and consumers through commercial and marketing support using an innovative approach across their value chain.
As a Medical Affairs Lead (IHS), you will be responsible for.
- Effectively leading the Medical Affairs activities for segment across therapy areas, providing effective business enablement and high edge scientific activities towards achieving disease and therapy area leadership and enhancing access of products in disease and therapy areas of interest.
- Helping in evaluation of New Products for therapy prominence working portfolio and strategy team and marketing team.
- Building connects with KOLs (Key Opinion Leaders) in shaping Therapy understanding and molecule understanding. CME/Ad board conduct ((Continuing Medical Education (CME)/(Medical) Advisory Board)), support guidelines, consensus etc.
- Having scientific activities those are considered differentiated and purposeful for targeted audience.
- Identifying need and planning evidence generation and post marketing studies.
- Guiding marketing teams in ensuring proper medical inputs and activities are delivered as per compliance.
- Medico-marketing Support
- Compliance in medico marketing activity
- Evidence generation activities
- Evaluation of New Products
- Training and Development
- Scientific Updates
- Activities for Digital Platforms & Other activities
- Support Medical writing , Publication and communication
What you already have.
- MD (Pharmacology/Medicine) / MBBS
Experience:
- 5-8 year in Medical Affairs -
- Freshers with exceptional academic qualifications will be considered
Skills:
- MS Office
- Excellent written & oral communication skills
- Disease/Therapy Knowledge
- Business Acumen
- Excellent Relationship Building Skills
- Broad Understanding of Medical Affairs
- Confidence to interact with Internal & External Stakeholders
Skills Required
Business Acumen, Ms Office
Regional Manager - Medical Affairs
Posted today
Job Viewed
Job Description
JOB DESCRIPTION - REGIONAL MEDICAL AFFAIRS MANAGER