41 Medical Communication jobs in India
Medical Affairs Manager
Posted 1 day ago
Job Viewed
Job Description
A Medical Affairs Manager will develop and execute medical strategies, ensuring scientific and regulatory compliance, and serving as a medical expert for internal and external stakeholders. Key responsibilities involve managing clinical trial activities, creating and approving promotional materials, and building relationships with healthcare professionals and key opinion leaders. They also collaborate with other departments, provide medical training, and oversee publication processes.
Core Responsibilities:
- Strategy and planning: Develop and implement medical strategies that align with the company's commercial and clinical goals.
- Medical expertise: Serve as a scientific and clinical expert, providing medical input on product development and strategy.
- Regulatory compliance: Ensure all medical content, activities, and materials comply with industry standards and regulations.
- Clinical trial management: Plan, coordinate, and oversee clinical trials, including investigator-initiated studies.
- Medical education: Develop and deliver medical education programs and scientific exchange events for internal teams and external healthcare professionals.
- Stakeholder engagement: Build and maintain relationships with key opinion leaders (KOLs), medical societies, academic institutions, and other external stakeholders.
- Cross-functional collaboration: Work closely with other departments like marketing, regulatory, and clinical development to provide medical insights.
- Content and publication oversight: Approve promotional materials and oversee the publication of scientific data in manuscripts, abstracts, and presentations.
- Training and support: Provide scientific and clinical training to internal teams
Key Skills and Qualifications:
- Advanced degree in a relevant scientific or medical field (e.g., MBBS, M.D.).
- Strong understanding of clinical research and regulatory requirements.
- Excellent communication, presentation, and interpersonal skills.
- Ability to collaborate effectively with cross-functional teams.
- Project management and leadership skills.
Medical Affairs Manager
Posted 5 days ago
Job Viewed
Job Description
Hansa Medcell is looking for a medico-marketing and medical communication professional who can blend medical knowledge with strategic and creative thinking to build strong brands. The role focuses on creating clear, engaging communication across clinics, digital channels, and events.
Role: Medical Lead
Experience: 6 - 8 Years
Qualification: Graduate or PG in related field
Key Responsibilities:
Strategic & Scientific Leadership
- Define scientific positioning and long-term brand strategy across lifecycle stages.
- Identify evidence gaps and guide publication, KOL, and CME strategies.
- Track competitor landscape, emerging science, and market insights to inform brand plans.
Content & Engagement Strategy
- Develop scientific and educational content for HCPs, patients, and internal teams.
- Plan and oversee in-clinic and digital marketing assets with scientific accuracy and relevance.
- Drive HCP and patient engagement through CMEs, webinars, digital campaigns, and social media.
Client & Project Leadership
- Act as the primary scientific and strategic partner to clients and internal teams.
- Lead projects end-to-end—strategy, content, execution, and delivery.
- Present recommendations confidently while managing timelines and cross-functional collaboration.
Interested candidates please share resumes at:
Medical Affairs Manager
Posted 22 days ago
Job Viewed
Job Description
Responsibilities:
- Develop and implement the strategic medical affairs plan for assigned products.
- Engage with and support Key Opinion Leaders (KOLs) and other healthcare professionals (HCPs) through scientific exchange.
- Provide scientific and medical expertise to internal teams, including marketing, sales, and R&D.
- Review and approve promotional and non-promotional materials to ensure scientific accuracy and regulatory compliance.
- Identify and support investigator-initiated studies (IIS) and collaborative research projects.
- Contribute to the development of clinical trial protocols and strategies.
- Present scientific data at medical congresses and advisory boards.
- Monitor the scientific and competitive landscape, providing insights to inform strategic decisions.
- Ensure adherence to all relevant industry codes, guidelines, and regulations.
- Contribute to the development of medical education programs.
- Advanced degree (MD, PharmD, PhD, or equivalent) in a relevant life science or medical field.
- Minimum of 5 years of experience in medical affairs, clinical development, or a related role within the pharmaceutical industry.
- In-depth knowledge of therapeutic areas relevant to the company's product portfolio.
- Proven experience in engaging with KOLs and building strong professional relationships.
- Excellent understanding of pharmaceutical product development, clinical data interpretation, and regulatory affairs.
- Strong communication, presentation, and interpersonal skills.
- Ability to think strategically and develop innovative medical plans.
- Proficiency in medical terminology and scientific writing.
- Experience in reviewing promotional materials is highly desirable.
- Willingness to travel as needed for scientific engagements and meetings.
Medical Affairs Partner, Oncology
Posted 2 days ago
Job Viewed
Job Description
**The Position**
**Position Based in Malaysia**
At Roche, we believe it's urgent to deliver medical solutions right now - even as we develop innovations for the future. We are passionate about improving the lives of patients' and are bold in both decision and action. We believe that partnering with health systems around the world can create value for patients, society and for Roche. We are uniquely positioned to realize truly integrated health solutions across pharmaceuticals, diagnostics, digital health and big data solutions; positioning us as a key partner for personalized, sustainable healthcare everywhere.
The Medical Affairs Partner (MAP) demonstrates personal purpose around improving the patient journey, as well as strong passion to create value and impact on the ecosystem. The MAP is a senior level role within the affiliate, who has decision making authority to request resources of Roche (both within the affiliate and broader network) in order to have improved impact on the patient journey.
They are a core member of the disease area pod working in close collaboration with the Patient Journey Partners (PJP). The MAP spends majority of their time in the field close to customers communicating the value of Roche's science and products to physicians, investigators and institutions. They think from an enterprise level, and will also be a member of an APAC level network working across borders, to realize and scale country outcomes by contributing to virtual, cross border, cross functional work package teams.
**The Opportunity:**
The Medical Affairs Partner has a reporting line to the Country Medical, Innovation and Regulatory Lead, serves the affiliate vision with an aligned mindset and behaviors.
+ Oversee the patient journey in its entirety, acts as a system thinker with the ability to identify shared purpose among stakeholders and cocreate with them to bring better outcomes for patients faster by translating insights into strategic and actionable recommendations.
+ Bring the inside out, to bring Roche expertise, science and knowledge to the ecosystem. Steward Roche's products through their lifecycle and supports their appropriate use, which includes sharing their merits with Healthcare Professionals (HCPs) in a truthful and balanced manner. Ensure great experiences whenever stakeholders in the ecosystem engage with Roche employees, products and services.
+ Pull in expertise and resources locally and from the network as needed, prioritize and drive solutions that deliver outcomes faster. Boldly act on key decisions and opportunities and boldly stop any activity that is not adding value.
+ Identify important data gaps and opportunities designing and supporting data generation plans to address them including phase IV studies, registries and real world evidence generation.
+ Hold an altruistic approach in supporting the global network.
+ Act as a leader, coach and mentor, who supports team working and actively contributes to the learning & development of peers across strategically aligned therapy areas, key medical affairs capabilities and engagement with healthcare professionals and patient groups.
+ Display integrity in all levels (i.e. open, honest, ethical and genuine). All Roche employees are expected to practice high standards of compliance with both external and internal policies andregulations as well as participate and be involved in SHE initiatives within the Company.
+ Supports GxP-related activities to ensure quality compliance requirements are adhered to
**Who You Are:**
+ Is self-managed and self-directed, ready to take on empowerment. Demonstrates a growth mindset, able to learn and unlearn quickly, take risks and experiment.
+ Has an enabler mindset leveraging the internal and external networks to create value, sharing back and scaling. Has outstanding partnering capabilities such as coaching, consulting, ability tolisten deeply, question and understand.
+ Willing to travel when needed.
Skills and Experience :
+ Has a deep understanding of patient journey and related treatments, medical affairs strategies & tactics including clinical research as well as broad understanding of Roche's present portfolio andfuture pipeline, such that they can work on future-based solutions. Is able to effectively sharescientific information including investigational findings through direct communications andengagement at scientific conferences with healthcare professionals and/or the scientific community.
+ Has excellent stakeholder engagement skills including partnering with Therapeutic Area Experts (TAEs) and organizations isrequired. Experience partnering with Patient Advocacy Group(PAGs) is highly desired.
+ Evidence generation skills is required. Supports relevant Product Development Medical Affairs (Global Medical Affairs) (PDMA) and Country Clinical Operationstrial, Early Access Program and Compassionate Use program activities within their diseasearea/ecosystem
+ Work efficiently and harmoniously in a cross-functional team, able to formulate cross-functionalstrategies and orchestrate cross-functional teams. Experience in agile ways of working is highlydesired.
+ Experience with medical review of promotional materials is required.
+ Ability to leverage digital means and tools is required.
+ Proficiency in English is required, fluency in the local language is desired.
+ Trained in GMP and GDP requirements for pharmaceutical
Education & Expertise:
+ Medical degree and/or PHD preferred, bachelor's degree in life sciences (eg. immunology,biomedical, biology or pharmacy) required.
+ Minimum of 3 years experience within a Medical Affairs role in Pharmaceutical, Diagnostics,Health Sciences, Biotechnology or other related fields is required.
+ Experience and expertise in **Oncology** , specifically HCC and Lung Cancer is preferred.
**Who we are**
A healthier future drives us to innovate. Together, more than 100'000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let's build a healthier future, together.
**Roche is an Equal Opportunity Employer.**
Medical Affairs Manager - Oncology
Posted 1 day ago
Job Viewed
Job Description
Key Responsibilities:
- Develop and implement comprehensive medical affairs plans for oncology products.
- Identify, engage, and cultivate relationships with Key Opinion Leaders (KOLs) in the oncology field.
- Provide scientific and clinical information support to internal teams and external stakeholders.
- Develop high-quality medical content, including presentations, publications, and educational materials.
- Organize and execute advisory boards, symposia, and scientific meetings.
- Collaborate with Clinical Development, R&D, Marketing, and Sales teams to ensure alignment of medical strategy.
- Review and approve medical and marketing materials for scientific accuracy and compliance.
- Contribute to the interpretation and communication of clinical trial data.
- Monitor the competitive landscape and identify emerging trends in oncology.
- Ensure adherence to all industry regulations and company policies.
- Advanced degree (M.D., Ph.D., Pharm.D., or equivalent) in a life sciences or healthcare-related field.
- Minimum of 5 years of experience in medical affairs, clinical development, or a related pharmaceutical role, with a focus on oncology.
- In-depth knowledge of oncology disease areas, treatment paradigms, and clinical research.
- Demonstrated ability to build and maintain strong relationships with KOLs.
- Excellent written and verbal communication, presentation, and interpersonal skills.
- Strong analytical and strategic thinking capabilities.
- Experience in medical writing and review of scientific/promotional materials.
- Ability to work effectively in a cross-functional team environment.
- Proficiency in MS Office Suite.
Senior Medical Affairs Manager
Posted 6 days ago
Job Viewed
Job Description
Key Responsibilities:
- Develop and implement comprehensive medical affairs strategies aligned with product development and commercial objectives.
- Identify, establish, and maintain strong, collaborative relationships with Key Opinion Leaders (KOLs) and other influential healthcare professionals.
- Provide scientific and clinical expertise to support the development of medical education programs, publications, and presentations.
- Review and approve promotional and non-promotional materials to ensure scientific accuracy and regulatory compliance.
- Support the planning and execution of Phase IV clinical trials, post-marketing studies, and real-world evidence generation.
- Act as a scientific liaison, presenting complex clinical data and addressing inquiries from healthcare professionals.
- Collaborate closely with cross-functional teams, including R&D, marketing, sales, and regulatory affairs, to ensure alignment and achieve strategic goals.
- Develop and manage the medical affairs budget for assigned therapeutic areas.
- Stay abreast of the latest scientific advancements, clinical research, and market trends within relevant therapeutic areas.
- Ensure all medical affairs activities are conducted in compliance with GxP, company policies, and relevant industry regulations.
- Contribute to the development of scientific exchange strategies and materials.
- Mentor and guide junior medical affairs professionals.
Lead Medical Affairs Specialist
Posted 12 days ago
Job Viewed
Job Description
Key Responsibilities:
- Develop and implement comprehensive medical affairs plans aligned with company objectives and product strategies.
- Engage with Key Opinion Leaders (KOLs), healthcare professionals (HCPs), and academic institutions to foster scientific exchange and collaboration.
- Provide scientific and medical input for product development, clinical trials, and post-market surveillance activities.
- Develop and review scientific and educational materials, ensuring accuracy, compliance, and clarity.
- Support the planning and execution of medical education programs, symposia, and advisory boards.
- Analyze and interpret clinical data, generating insights to inform medical strategy and communications.
- Ensure adherence to all relevant regulatory guidelines, ethical standards, and internal policies.
- Collaborate with cross-functional teams, including R&D, Marketing, and Regulatory Affairs, to ensure seamless integration of medical affairs activities.
- Monitor the competitive landscape and emerging scientific trends within relevant therapeutic areas.
- Contribute to the training and development of other medical affairs team members.
Qualifications:
- Advanced degree (MD, PhD, PharmD, or equivalent) in a relevant scientific or medical discipline.
- Minimum of 7 years of experience in medical affairs within the pharmaceutical or biotechnology industry.
- Demonstrated expertise in strategic planning and execution of medical affairs initiatives.
- Proven experience in building and managing relationships with KOLs and HCPs.
- Strong understanding of clinical research, drug development processes, and regulatory requirements.
- Exceptional scientific communication, presentation, and writing skills.
- Ability to critically evaluate scientific literature and data.
- Excellent project management and organizational skills.
- Proficiency in relevant therapeutic areas is highly desirable.
- Self-starter with a proven ability to work independently and effectively in a remote setting.
This is a unique opportunity to shape the medical narrative for innovative therapies from the comfort of your home office. If you are passionate about advancing medical science and possess the requisite expertise, we encourage you to apply for this remote-first role.
Be The First To Know
About the latest Medical communication Jobs in India !
Senior Medical Affairs Manager
Posted 14 days ago
Job Viewed
Job Description
Responsibilities:
- Develop and implement comprehensive medical affairs strategies aligned with corporate objectives.
- Identify, build, and maintain strong relationships with Key Opinion Leaders (KOLs) and other stakeholders in relevant therapeutic areas.
- Lead the planning and execution of medical education programs, symposia, and advisory boards.
- Contribute to the development of clinical trial protocols and study designs.
- Review and approve promotional and non-promotional materials for scientific accuracy and compliance.
- Provide scientific and medical expertise to internal teams, including marketing, sales, and R&D.
- Stay abreast of the latest scientific developments, clinical research, and competitive landscape within assigned therapeutic areas.
- Oversee the generation and dissemination of scientific data and publications.
- Manage the medical affairs budget and resources effectively.
- Ensure adherence to all relevant industry regulations, ethical guidelines, and company policies.
- Support product launches and lifecycle management from a medical perspective.
- Represent the company at scientific congresses and meetings.
- Advanced degree (MD, PhD, PharmD, or equivalent) in a relevant scientific or medical discipline.
- Minimum of 7 years of experience in medical affairs within the pharmaceutical industry, with a proven track record of success.
- Deep understanding of clinical development, evidence-based medicine, and regulatory affairs.
- Extensive experience in engaging with KOLs and managing medical communication strategies.
- Strong knowledge of assigned therapeutic areas.
- Excellent scientific and medical communication skills, both written and verbal.
- Demonstrated leadership and project management capabilities.
- Ability to think strategically and translate scientific data into actionable plans.
- Strong understanding of compliance and ethical guidelines in the pharmaceutical industry.
- Ability to travel domestically and internationally as required.
Lead Medical Affairs Specialist
Posted 19 days ago
Job Viewed
Job Description
Responsibilities:
- Develop and execute strategic medical affairs plans in alignment with product development and commercial objectives.
- Serve as a primary scientific and medical resource for assigned therapeutic areas.
- Identify, establish, and maintain relationships with key opinion leaders (KOLs) and other medical experts.
- Develop and deliver high-quality scientific and medical information to healthcare professionals through various channels (e.g., presentations, publications, advisory boards).
- Support the development of medical education materials and programs.
- Review and approve promotional and non-promotional materials for scientific accuracy and compliance.
- Collaborate with cross-functional teams, including R&D, marketing, sales, and regulatory affairs, to ensure cohesive strategies.
- Analyze and interpret clinical data to provide insights and support evidence-based decision-making.
- Contribute to the planning and execution of medical advisory boards and scientific meetings.
- Ensure all activities comply with relevant industry regulations, ethical guidelines, and company policies.
- Advanced degree (M.S., Ph.D., Pharm.D., M.D.) in a relevant scientific or clinical discipline.
- Minimum of 7 years of experience in medical affairs, clinical research, or a related scientific role within the pharmaceutical industry.
- In-depth knowledge of assigned therapeutic areas and a strong understanding of clinical trial design and interpretation.
- Proven experience in engaging with Key Opinion Leaders (KOLs) and managing relationships with medical experts.
- Excellent written and verbal communication skills, with the ability to present complex scientific information clearly and persuasively.
- Strong understanding of pharmaceutical regulations and compliance requirements.
- Demonstrated ability to work independently and collaboratively within a team environment.
- Strategic thinking and excellent project management skills.
- Ability to travel as needed for scientific meetings and KOL engagement.
- A passion for advancing patient care through scientific exchange.
Lead Medical Affairs Manager
Posted 22 days ago
Job Viewed
Job Description
Key Responsibilities:
- Develop and execute strategic medical affairs plans aligned with company objectives and therapeutic area priorities.
- Lead the development of medical communication materials, including scientific publications, presentations, and educational programs.
- Engage with Key Opinion Leaders (KOLs) and healthcare professionals to gather insights, share scientific information, and foster collaborative relationships.
- Oversee the medical review process for promotional and non-promotional materials, ensuring scientific accuracy and compliance with regulations.
- Provide medical expertise and support to cross-functional teams, including marketing, sales, regulatory, and R&D.
- Monitor the competitive landscape and emerging scientific trends within the therapeutic area.
- Manage the budget and resources allocated to medical affairs activities.
- Ensure adherence to all relevant industry codes, guidelines, and company policies.
- Contribute to the development of clinical trial protocols and scientific advisory boards.
- Mentor and develop junior members of the medical affairs team.
Qualifications:
- Advanced scientific or medical degree (MD, PharmD, PhD) or equivalent.
- Minimum of 7-10 years of progressive experience in pharmaceutical medical affairs, clinical research, or a related field.
- Proven experience in developing and implementing medical strategy.
- Deep understanding of the pharmaceutical industry, regulatory requirements, and ethical guidelines.
- Excellent scientific writing, presentation, and communication skills.
- Demonstrated ability to build and maintain strong relationships with healthcare professionals and KOLs.
- Strong leadership and team management capabilities.
- Ability to work independently and effectively in a remote, collaborative environment.
- Proficiency in data analysis and interpretation of clinical data.
- Experience in (Specific Therapeutic Area, e.g., Oncology, Cardiology) is a significant advantage.
This fully remote position offers the flexibility to work from anywhere in India, providing a unique opportunity to make a significant impact on medical strategy while maintaining a healthy work-life balance. We are looking for a dedicated and strategic thinker to join our client's growing team.