1,542 Medical Communications jobs in India

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.

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.

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:

• 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.

• 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.

• 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.

• 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.

• 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.