649 Indian Council Of Medical Research jobs in India

**Primary Duties**
- Serve as a field-based extension of the Therapeutic Area Medical Strategy Group
- Systematically identify the scientific exchange needs of Key Opinion Leaders (KOLs), investigators and other stakeholders in patient care, establish strong professional relationships, provide credible scientific expertise and serve as a liaison to Takeda Global Medical, Global Clinical and external partners
- Ensure compliant communication and education of Takeda’s marketed and emerging product portfolio to meet the educational and professional needs of Takeda’s key customers
- Responds effectively to requests for scientific exchange
- Support local team disease area and product knowledge through scientific training
- Maintain personal expertise in relevant disease areas and MSL best practices

**Responsibilities**

Job Function and Description

40% of time

KOL Relationship Management:

- Through compliant scientific exchange, builds and maintains professional relationships with external stakeholders to expand Takeda’s research, advisory and educational partnership opportunities
- Ensures high standard of professionalism to develop and maintain “peer-to-peer” scientific relationships with key thought leaders in healthcare, academia, payer, and government organizations per strategic territory plans and as requested by KOLs, including the management of strategic scientific partnerships and scientific exchange
- Provide scientific liaison support to Investigators currently involved in the Takeda’s Company sponsored interventional or observational studies and investigator-initiated trials
- Engage KOLs through various planned scientific activities, to increase awareness on disease perception for TA as per Takeda norms and SOPs
- Facilitate 1:1 and group scientific interactions with healthcare professionals
- Maintain KOL profile, plans and insights including updating medical customer relationship management system in a timely, accurate, and compliant manner
- Maintain awareness of and access to internal and external information sources available to support high-quality scientific exchange, and coordinate high-quality interactions between these resources and external customers

40% of time

Effective and Compliant Dissemination of Data including HCP education and disease awareness
- Presents clinical and disease state information to a variety of audiences, including KOLs, Medical advisors, formulary/decision makers and other HCPs and Takeda internal teams
- Respond within defined timeline and quality standards to unsolicited inquiries from HCPs and other stakeholders received by Global Medical Affairs
- Drive, support and execute presentation of scientific evidence and medical education amongst physician community in assigned TA
- Ensures appropriate scientific exchange with HCPs by fostering fair and balanced medical and scientific communications that are not misleading
- Serves as scientific resource at key medical, scientific, and patient advocacy conferences as assigned
- Conducts therapeutic training for Sales and Medical colleagues upon request

10% of time

Contribute to Takeda’s Strategic Medical Strategy
- Provide scientific input and participate in local medical and cross-functional initiatives
- Provide field-based medical support to Takeda’s clinical research programs, registries, and facilitation of the investigator sponsored trials process
- Communicates key medical insights from KOLs/HCPs to inform refinement of medical strategies or tactics
- Gains customer insights, opinions and feedback and engages with internal colleagues to connect business opportunities with internal resources
- Under the guidance of _(MSL Team Lead or Region Lead)_, provides scientific support for company-sponsored meetings
- Participates on internal project teams as directed by Management (e.g. publications)

10% of time

Maintaining personal expertise in relevant disease areas and MSL best practices
- Maintain knowledge base and scientific expertise on all assigned Takeda disease areas and products
- Develop and update knowledge of applicable pharmaceutical guidelines and regulations, including, but not limited to, ICH, GCP, PhRMA, DOJ, OIG, R&D Code of Ethical Practices and company policies
- Develop/increase knowledge of medical literature and critical appraisal of scientific publications

**Education and Experience Requirements**
- MBB/MD/Advanced degree in life sciences (PhD) is required
- Medical affairs, clinical or research experience in the assigned disease area is preferred
- Demonstrative therapeutic experience/research or substantive patient care experience is preferred (2 years minimum)
- Demonstration of expertise in key skills and competencies

**Key Skills, Abilities, and Competencies**
- Communication/presentation skills - Able to exchange scientific ideas and information openly and effectively with key opinion leaders and with colleagues
- Relationship-building & Engagement - Able to man

**At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.**

**Medical Science Liaison**

**Roles and Responsibilities**

**Primary Activities**:

- Exchange and dissemination of scientific, educational, and research related information:
The MSL plans, prepares and engages with Thought Leaders (TLs - Doctors) as an information scientist and colleague both proactively and reactively via various innovative TL engagements tactics and formats. MSLs provide dissemination, clarification and education of scientific data, study protocols, meeting abstracts, and professional literature (both proactive discussions on-label, and reactive discussions for unsolicited off-label questions in alignment with local regulations).
- Interactions with Medical Societies and Advisory Boards:
The MSL answers medical / scientific queries of Medical Societies with regards to Bayer products and organizes / supports / participates in advisory boards.
- Participation at / networking in Congresses and Conventions:
The MSL attends congresses and conventions, interacts with TLs (Doctors), establishes new contacts and gathers competitive intelligence.
- Coordination of Scientific Education Activities:
The MSL plans and organizes scientific training and education events / sessions with TLs within their specific therapeutic area or product.
- TL identification / profiling / segmentation and strategy and engagement planning:
In alignment with product Medical Affairs plan, the MSL contributes to internal understanding of specific TL interests and expertise within the medical community at large.

6. Preparation of reports and tracking activities:
The MSL submits timely reports and tracks activities against agreed objectives

**Secondary Activities**:
External scientific support, training and education: The MSL provides additional external scientific support, training & education not covered by other primary activities.

**Who you are**:

- Qualification in natural sciences, or Medical background (MD/ MBBS/BAMS/ BDS/ MDS)
- Basic knowledge of the concerned therapy area (women’s health, contraception, endometriosis) and related molecules
- Basic understanding of clinical trials, their design, and rationale.
- Ability to work independently as well as in a team environment and to build productive work relationships both internally and externally
- Excellent presentation and written and verbal communication skills

**Bayer does not charge any fees whatsoever for recruitment process. Please do not entertain such demand for payment by any individuals / entities in connection with recruitment with any Bayer Group entity(ies) worldwide under any pretext.**

**YOUR APPLICATION**

**Location**:

- India : West Bengal : Kolkata

**Division**:

- Pharmaceuticals

**Reference Code**:

- 844460

**Contact Us**
- + 022-25311234

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
Medical Science Liaison, Oncology
Develops and maintains professional relationships with internal and external customers to provide comprehensive medical and scientific support to Abbvie initiatives in assigned therapeutic areas.
Executes against the Medical Affairs plan for India. Provides scientific education and training initiatives across Abbvie Oncology portfolio. Plans and leads scientific communication with key therapy leaders and stakeholders, organizing advisory board meetings, facilitating clinical trials, and serving as the medical resource for both external and internal stakeholders. This position is a non-promotional role. The primary focus is providing Healthcare Professionals with fair and balanced scientific information.
Facilitates information, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies in development or commercialized by Abbvie. Works closely with other Abbvie personnel to ensure information, education, and research needs of healthcare professionals are met and to ensure scientific and technical training needs of commercial organizations are identified and met.
Key Responsibilities Area
As an internal medical / technical / scientific resource, leads medical affairs objectives in the affiliate country. The role requires competency in practical aspects of patient care, and the ability to use medical and scientific information to facilitate engagement of physicians and others in the clinical and basic scientific issues relevant to Abbvie's products.
Responsible for maintaining annual expenses within assigned budget parameters.
Responsible for accurate and timely documentation of medical lead activities.
The employee must conduct their work activities in compliance with all Abbvie internal requirements and with all applicable regulatory requirements. Abbvie internal requirements include compliance with ethics, environmental health and safety, financial, human resources, and general business policies, requirements and objectives.
Identify, develop and maintain professional relationships with thought leaders, academic centers and researchers in assigned areas of therapeutic interest to ensure access to current medical and scientific information on Abbvie products.
Work closely with the Commercial leaders for business planning , Therapeutic leads & Dir, Medical Affairs to set priorities, and activities.
Upon request, present data on Abbvie products to healthcare professionals including physicians, academic institutions, researchers, and other health care professionals.
Support research initiatives as requested by Abbvie R&D, Clinical Operations, and Medical Affairs Departments.
Serve as internal medical and scientific resource to assigned Abbvie therapeutic areas for development of disease-state and product communications and materials that are medically accurate, balanced, and consistent with regulatory guidelines.
Support Round Table and Advisory Board sessions to ensure accuracy of scientific and clinical data.
Conducts on-going training to medical affairs, field sales and other internal personnel as required.
A high level of travel / field time is to be expected within this position (approximately 60% of time spent outside the office). This role will also serve as the local representative of the Global Medical Office associated functions. (eg PV, HEOR etc)
Qualifications
Qualifications
Requirements
Minimum 2-3 years post-qualification work experience in Medical affairs function.
Experience working within the pharmaceutical industry or within clinical research is preferred
Experience of working collaboratively and cross-functionally in a matrix structure, supporting multiple stakeholders
Demonstrated ability to learn quickly and convey clinical and non-clinical technical information effectively to individuals with varying degrees of scientific acumen.
Demonstrated strong presentation and teaching skills with ability to effectively share information with others
Demonstrated ability to develop and maintain strong relationships; to lead & engage
Experience applying analytical skills, to critically evaluate and effectively communicate key clinical data
Experience working with technology, including systems such as Microsoft Office.
Education
MD;
MBBS
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community? Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

**Primary Duties**
- Serve as a field-based extension of the Therapeutic Area Medical Strategy Group
- Systematically identify the scientific exchange needs of Key Opinion Leaders (KOLs), investigators and other stakeholders in patient care, establish strong professional relationships, provide credible scientific expertise and serve as a liaison to Takeda Global Medical, Global Clinical and external partners
- Ensure compliant communication and education of Takeda’s marketed and emerging product portfolio to meet the educational and professional needs of Takeda’s key customers
- Responds effectively to requests for scientific exchange
- Support local team disease area and product knowledge through scientific training
- Maintain personal expertise in relevant disease areas and MSL best practices

**Responsibilities**

Job Function and Description

40% of time

KOL Relationship Management:

- Through compliant scientific exchange, builds and maintains professional relationships with external stakeholders to expand Takeda’s research, advisory and educational partnership opportunities
- Ensures high standard of professionalism to develop and maintain “peer-to-peer” scientific relationships with key thought leaders in healthcare, academia, payer, and government organizations per strategic territory plans and as requested by KOLs, including the management of strategic scientific partnerships and scientific exchange
- Provide scientific liaison support to Investigators currently involved in the Takeda’s Company sponsored interventional or observational studies and investigator-initiated trials
- Engage KOLs through various planned scientific activities, to increase awareness on disease perception for TA as per Takeda norms and SOPs
- Facilitate 1:1 and group scientific interactions with healthcare professionals
- Maintain KOL profile, plans and insights including updating medical customer relationship management system in a timely, accurate, and compliant manner
- Maintain awareness of and access to internal and external information sources available to support high-quality scientific exchange, and coordinate high-quality interactions between these resources and external customers

40% of time

Effective and Compliant Dissemination of Data including HCP education and disease awareness
- Presents clinical and disease state information to a variety of audiences, including KOLs, Medical advisors, formulary/decision makers and other HCPs and Takeda internal teams
- Respond within defined timeline and quality standards to unsolicited inquiries from HCPs and other stakeholders received by Global Medical Affairs
- Drive, support and execute presentation of scientific evidence and medical education amongst physician community in assigned TA
- Ensures appropriate scientific exchange with HCPs by fostering fair and balanced medical and scientific communications that are not misleading
- Serves as scientific resource at key medical, scientific, and patient advocacy conferences as assigned
- Conducts therapeutic training for Sales and Medical colleagues upon request

10% of time

Contribute to Takeda’s Strategic Medical Strategy
- Provide scientific input and participate in local medical and cross-functional initiatives
- Provide field-based medical support to Takeda’s clinical research programs, registries, and facilitation of the investigator sponsored trials process
- Communicates key medical insights from KOLs/HCPs to inform refinement of medical strategies or tactics
- Gains customer insights, opinions and feedback and engages with internal colleagues to connect business opportunities with internal resources
- Under the guidance of _(MSL Team Lead or Region Lead)_, provides scientific support for company-sponsored meetings
- Participates on internal project teams as directed by Management (e.g. publications)

10% of tim

Maintaining personal expertise in relevant disease areas and MSL best practices
- Maintain knowledge base and scientific expertise on all assigned Takeda disease areas and products
- Develop and update knowledge of applicable pharmaceutical guidelines and regulations, including, but not limited to, ICH, GCP, PhRMA, DOJ, OIG, R&D Code of Ethical Practices and company policies
- Develop/increase knowledge of medical literature and critical appraisal of scientific publications

**Education and Experience Requirements**
- MBB/MD/Advanced degree in life sciences (PhD) is required
- Medical affairs, clinical or research experience in the assigned disease area is preferred
- Demonstrative therapeutic experience/research or substantive patient care experience is preferred (2 years minimum)
- Demonstration of expertise in key skills and competencies

**Key Skills, Abilities, and Competencies**
- Communication/presentation skills - Able to exchange scientific ideas and information openly and effectively with key opinion leaders and with colleagues
- Relationship-building & Engagement - Able to mana

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

**Role Summary**:
MSLs’ embody our medical mission in becoming a trusted, agile partner who engages in relevant dialogue and delivers timely, high impact data and insights that advance the science or accelerate access, optimize medical practice and drive appropriate adoption of BMS medicines. The MSL role is a field-based role. It is anticipated that a MSL will spend a minimum of 60-70% of their time in the field with external customers.

The primary role of an MSL is to develop and maintain contacts with Thought Leaders (TL) and Healthcare Providers (HCP) within their healthcare system. The purpose of interactions is to ensure patients have access to BMS medicines, to ensure their safe and appropriate use through peer to peer discussions aligned with medical strategies and needs expressed by the stakeholders. The scientific dialogue focuses on scientific/clinical information around disease management and BMS products in a fair and balanced way and includes appropriate Health Economics and Outcomes Research (HEOR) data.

**Key responsibilities**:
1. External Environment and Customer Focus
- Develop and maintain interactions with Thought Leaders, appropriate HCPs, and access stakeholders, within a given geography to answer scientific, unsolicited product and HEOR related questions. MSLs will use various channels for interactions (1:1, group presentation; remote, etc).
- Develop and execute a medical interaction plan with Key accounts (Army, Railways, CGHS etc.) as per the needs of the stakeholders and the overall medical strategy
- Effectively present information to HCPs and be able to respond to questions, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives.
- Actively assess the medical landscape by meeting with Thought Leaders to understand their needs and expertise. Continuously update their own knowledge in treatment strategies, products, unmet medical needs, clinical trials and scientific activities. Understand the competitive landscape and actively prepare to address informational needs of customers.
- Collect and provide meaningful medical insights back to the medical and commercial organizations to be actioned in support of the strategy development.
- Report safety information, including adverse events, in accordance with BMS Standard Operating Procedures.

2. Contribute to the Medical Plan
- Develop territory Field Medical plan and TL Interaction plans based on therapeutic area objectives and TLs needs.
- Execute certain medical plan activities as assigned.
- Adopt institution/account planning approach and contribute to cross-functional institution/account plans.
- Contribute to development and delivery of scientifically meaningful medical programs/projects in line with the local Medical and Field Medical plan.

3. Provide Medical Support
- As necessary and appropriate, support the initial and ongoing medical/scientific area and product specific training and provide key scientific updates to internal stakeholders (e.g. Commercial, Regulatory, Pharmacovigilance, Legal, HEOR, Market Access).
- Provide scientific support at promotional meetings by presenting unbiased scientific and clinical data, by evaluating speakers and by giving support to BMS-contracted speakers.

4. Support Clinical Trial Activities
- Support Interventional and Non Interventional Research (NIR) studies (e.g. identification and assessment of potential study sites) to support patient recruitment and/or discussions around the safe and effective use of BMS investigational products, as agreed with local medical management and as defined by the study scope document.
- Provide recommendations and insights to clinical development team on study and site feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators, as agreed with local medical management.
- Actively support CRO sponsored studies as agreed with local medical management and as defined by the study scope document.
- Support HCPs in the ISR submission process as agreed with local medical management.
- Ensure that BMS Pharmacovigilance procedural documents are understood and applied by investigators of local studies, and alert appropriate BMS personnel to any identified Adverse Events.

5. Contribute towards the Patient advocacy programs
- Support the implementation of the patient education programs in collaboration with the patient advocacy groups
- Support the creation of patient education materials

**Qualifications**:

- MBBS, MD, BDS

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

**Role Summary**:
MSLs’ embody our medical mission in becoming a trusted, agile partner who engages in relevant dialogue and delivers timely, high impact data and insights that advance the science or accelerate access, optimize medical practice and drive appropriate adoption of BMS medicines. The MSL role is a field-based role. It is anticipated that a MSL will spend a minimum of 60-70% of their time in the field with external customers.

The primary role of an MSL is to develop and maintain contacts with Thought Leaders (TL) and Healthcare Providers (HCP) within their healthcare system. The purpose of interactions is to ensure patients have access to BMS medicines, to ensure their safe and appropriate use through peer to peer discussions aligned with medical strategies and needs expressed by the stakeholders. The scientific dialogue focuses on scientific/clinical information around disease management and BMS products in a fair and balanced way and includes appropriate Health Economics and Outcomes Research (HEOR) data.

**Key responsibilities**:
1. External Environment and Customer Focus
- Develop and maintain interactions with Thought Leaders, appropriate HCPs, and access stakeholders, within a given geography to answer scientific, unsolicited product and HEOR related questions. MSLs will use various channels for interactions (1:1, group presentation; remote, etc).
- Develop and execute a medical interaction plan with Key accounts (Army, Railways, CGHS etc.) as per the needs of the stakeholders and the overall medical strategy
- Effectively present information to HCPs and be able to respond to questions, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives.
- Actively assess the medical landscape by meeting with Thought Leaders to understand their needs and expertise. Continuously update their own knowledge in treatment strategies, products, unmet medical needs, clinical trials and scientific activities. Understand the competitive landscape and actively prepare to address informational needs of customers.
- Collect and provide meaningful medical insights back to the medical and commercial organizations to be actioned in support of the strategy development.
- Report safety information, including adverse events, in accordance with BMS Standard Operating Procedures.

2. Contribute to the Medical Plan
- Develop territory Field Medical plan and TL Interaction plans based on therapeutic area objectives and TLs needs.
- Execute certain medical plan activities as assigned.
- Adopt institution/account planning approach and contribute to cross-functional institution/account plans.
- Contribute to development and delivery of scientifically meaningful medical programs/projects in line with the local Medical and Field Medical plan.

3. Provide Medical Support
- As necessary and appropriate, support the initial and ongoing medical/scientific area and product specific training and provide key scientific updates to internal stakeholders (e.g. Commercial, Regulatory, Pharmacovigilance, Legal, HEOR, Market Access).
- Provide scientific support at promotional meetings by presenting unbiased scientific and clinical data, by evaluating speakers and by giving support to BMS-contracted speakers.

4. Support Clinical Trial Activities
- Support Interventional and Non Interventional Research (NIR) studies (e.g. identification and assessment of potential study sites) to support patient recruitment and/or discussions around the safe and effective use of BMS investigational products, as agreed with local medical management and as defined by the study scope document.
- Provide recommendations and insights to clinical development team on study and site feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators, as agreed with local medical management.
- Actively support CRO sponsored studies as agreed with local medical management and as defined by the study scope document.
- Support HCPs in the ISR submission process as agreed with local medical management.
- Ensure that BMS Pharmacovigilance procedural documents are understood and applied by investigators of local studies, and alert appropriate BMS personnel to any identified Adverse Events.

5. Contribute towards the Patient advocacy programs
- Support the implementation of the patient education programs in collaboration with the patient advocacy groups
- Support the creation of patient education materials

**Qualifications**:

- MBBS, MD, BDS

**Roles and Responsibilities**
- Build a Win-win relationship with Regional KOLs, National KOLs in region, Key HCPs, via Scientific activities and Medical initiatives or programme execution
- Broaden the composition of Scientific experts on various concepts, products
- Speaker identification, creating opportunity for new speaker development and rising stars in the field of Women’s Health/Gynaceology, or Critical Care &, Emergency medicine (or other fields), leveraging the opportunity to Business
- Active involvement in Medical insights gathering and sharing, Market Research, New Products, Concept Advocacy, Clinical Data Generation, wherever/ whenever needed.
- Regional owner of medical and scientific, medico-marketing activities, in compliance with applicable codes and company policies
- Conceptualizing and Driving one dedicated Regional level Project involving various stakeholders and support other HO lead Business Projects with Medical inputs
- Execution of Medical affairs strategies and plans for Key Products in assigned therapy areas in the region
- Cross-functional collaboration with Marketing, Sales and others to drive Product Strategy, Communications Strategy with External Stakeholders for respective regions
- Program related: Preparation and participation in various Medical symposium/events “Key-Speaker-Training” activities (Focus groups or Expert Meetings)
- Communication related: Develop and present medical and scientific communication; communication of safety-related topics for all key products
- Lead and conduct New Product and disease area/therapy Trainings for Sales and Marketing teams, basic, advanced and refresher training program for the regional representatives or sometimes for all
- Role:
Medical Officer
- Salary:
Not Disclosed by Recruiter
- Industry:
Pharmaceutical & Life Sciences
- Functional Area:
Healthcare & Life Sciences
- Role Category:
Doctor
- Employment Type:
Full Time, Permanent
- Key Skills

Regional KOLs National KOL

medical science liaison

Gynaceology

Critical Care

Medical

regional medical advisor
- Education
- UG:
MBBS in Any Specialization
- PG:
Medical-MS/MD in Any Specialization

Company Profile
- Bharat Serums and Vaccines
- Our belief in Bringing Life to Life is anchored to a passion that has made us preserve, protect and enhance quality of life. For over four decades, we at BSV have used scientific resources to develop a range of biological, biotech and pharmaceutical products. Today, we have the privilege of working in close partnership with our customers and stakeholders to make a sustainable impact.
- You are empowered to drive BSV's vision:

- We want to be a leading biopharmaceutical company driven by people and science to set benchmarks in patient outcomes across therapy areas of Women’s Health, Critical Care and Emergency Medicine.

Heliyon Associate Scientific Editor

Your new role:
Are you passionate about sharing accurate and valuable research results for the benefit of science, society, and the authors? If so, we have the perfect opportunity for you as an Associate Scientific Editor focusing on our medical science sections in
_Heliyon, _an open access journal (part of Cell Press). We are looking for a scientist with a broad academic interest in medical science who is keen on supporting scientists to publish their research in effective ways. This job offers a unique opportunity to start your editorial career with an exciting journal, which you can help shape and develop to ensure its scientific and commercial success.

Key responsibilities will include:

- Actively managing the peer review and publication process of assigned manuscripts in a growing open access journal
- Actively working with the _Heliyon_ team to develop the journal’s processes and content
- Building effective working relationships with colleagues across Cell Press and Elsevier
- You will also have the opportunity to be a stakeholder in innovative Cell Press and Elsevier initiatives that shape the future of science communication.
- This is a full-time editorial position based in our Chennai office.
- In future, this position may require travel to conferences to engage with researchers.

What you should bring:

- A relevant doctoral degree in the medical science.
- Deep knowledge and research experience in infectious diseases/global health/public health/immunology/nutrition, and a willingness to learn about and work on the other sections like cancer research, medicine, microbiology, oncology, pharmaceutical science, pharmacology, sports medicine/rehabilitation, and toxicology. Knowledge/experience in medical ethics/study design/trial registration will be an added advantage.
- Broad scientific interests and a passion for helping scientists publish their work.
- Strong organizational skills, and the ability to prioritize, focus, and achieve desired goals.
- Creativity, decisiveness, attention to detail, willingness to experiment, and a continuous improvement mindset.
- Customer-focused and attentive with good written and verbal communication skills in English.
- Excellent interactive and team working skills as well as the ability to work independently.
- Emphasis on quality and monitoring of all aspects of day-to-day publishing operations and actively address improvements where required.

What we offer:
Cell Press offers an attractive salary and benefits package and a stimulating working environment that encourages innovation. Applications will be held in the strictest of confidence.

Please include a cover letter describing why you are interested in the job and how your skills and knowledge could contribute the success of
_Heliyon_.Please read our

**At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.**

**Medical Science Liaison - Diabetes Care**

**Roles and Responsibilities**

**Primary Activities**:

- Exchange and dissemination of scientific, educational, and research related information:
The MSL plans, prepares and engages with Thought Leaders (TLs - Doctors) as an information scientist and colleague both proactively and reactively via various innovative TL engagements tactics and formats. MSLs provide dissemination, clarification and education of scientific data, study protocols, meeting abstracts, and professional literature (both proactive discussions on-label, and reactive discussions for unsolicited off-label questions in alignment with local regulations).
- Interactions with Medical Societies and Advisory Boards:
The MSL answers medical / scientific queries of Medical Societies with regards to Bayer products and organizes / supports / participates in advisory boards.
- Participation at / networking in Congresses and Conventions:
The MSL attends congresses and conventions, interacts with TLs (Doctors), establishes new contacts and gathers competitive intelligence.
- Coordination of Scientific Education Activities:
The MSL plans and organizes scientific training and education events / sessions with TLs within their specific therapeutic area or product.
- TL identification / profiling / segmentation and strategy and engagement planning:
In alignment with product Medical Affairs plan, the MSL contributes to internal understanding of specific TL interests and expertise within the medical community at large.
- Preparation of reports and tracking activities:
The MSL submits timely reports and tracks activities against agreed objectives

**Secondary Activities**:
External scientific support, training and education: The MSL provides additional external scientific support, training & education not covered by other primary activities.

**Who you are**:

- Qualification in natural sciences, or Medical background (MD/ MBBS/BAMS/ BDS/ MDS)
- Basic knowledge of the concerned therapy area (Chronic Kidney Disease and Diabetes) and related molecules
- Basic understanding of clinical trials, their design, and rationale.
- Ability to work independently as well as in a team environment and to build productive work relationships both internally and externally
- Excellent presentation and written and verbal communication skills

**Bayer does not charge any fees whatsoever for recruitment process. Please do not entertain such demand for payment by any individuals / entities in connection with recruitment with any Bayer Group entity(ies) worldwide under any pretext.**

**YOUR APPLICATION**

**Location**:

- India : Maharashtra : Mumbai**Division**:

- Pharmaceuticals**Reference Code**:

- 816184**Contact Us**
- + 022-25311234