7 Medical Strategy Jobs

As the Head of Medical Affairs at Bayer in India, your role is pivotal in contributing to the development of medical strategy and providing medical guidance and governance for the therapeutic area. You will lead, develop, and manage the medical team responsible for CH department support, ensuring the highest standard of scientific input into Brand Strategies. Your responsibilities include acting as the primary contact person for medical and scientific aspects of the drugs, providing expertise on medical governance, and overseeing the conduct of clinical trials and commercial activities while adhering to local regulations and Bayer SOPs. In this role, you will be responsible for ensuring adherence to the code of compliance by reviewing all activities related to pharmaceutical and OTC products, approving promotional materials, and overseeing medical personnel training. You will also manage and implement all medical activities for CH Medical Affairs, including budget planning and monitoring. As a member of the Consumer Health Leadership Team, you will contribute to strategic decision-making processes, develop local medical strategies, and establish scientific relationships with external stakeholders. Collaboration with cross-functional teams, promotion of medical-marketing strategies, and providing scientific leadership to the business unit are key aspects of your role. To excel in this position, you should have a degree in Medicine/Pharmacy/PhD, at least 10-15 years of work experience in the Consumer/OTC sector, and expertise in therapeutic areas covered by Bayer. Strong communication, organizational, and interpersonal skills are essential, along with the ability to work effectively in both local and global teams. You should also demonstrate a focus on achieving goals, continuous improvement, and the establishment of relationships with Thought Leaders. If you are looking to make a real difference in the medical field, drive strategic decisions, and contribute to the success of Bayer's Consumer Health division, this role offers a unique opportunity to showcase your expertise and leadership in medical affairs. Please note that unsolicited emails from addresses not ending with the domain name bayer.com or job advertisements redirecting to non-bayer.com email addresses should not be considered official communications. Location: India : Maharashtra : Thane Division: Consumer Health Reference Code: 841425 For further information, please contact us at +022-25311234.,

As a Medical Advisor, you will play a crucial role in providing the scientific foundation for the Therapeutic Area (TA) medical strategy. Your responsibilities will include overseeing various medical activities, engaging key thought leaders, and contributing to the development of the Medical Affairs strategic plan for the identified TA and products. You will serve as a core scientific member of the cross-functional franchise team, ensuring that the TA medical strategy is based on sound scientific principles. This will involve conceptualizing and managing a wide range of medical activities such as research, publications, medical education, and patient support programs in alignment with the TA Medical strategy. Engaging key thought leaders through medical affairs activities will be a key aspect of your role, contributing to the overall strategic plan. You will work closely with Regional Medical Affairs to execute the strategic medical affairs plan effectively, including activities related to medical education, product education, and special projects. In your capacity as a Medical Advisor, you will act as a therapeutic area scientific expert, engaging in discussions on scientific data with specialists and providing training on the latest medical developments to the sales and marketing team. Your expertise and insights will be instrumental in driving the success of medical initiatives within the organization. To qualify for this role, you should hold an MBBS with M.D. Pharmacology/Medicine or a full-time post-graduate qualification in any discipline of medicine. Additionally, you should have a minimum of 2-4 years of experience in the pharmaceutical industry or a research company in a Medical Advisor capacity. Your prior experience and educational background will equip you with the necessary skills to excel in this challenging yet rewarding position.,

VeCura Wellness is India's first and only chain of scientific slimming and wellness clinics dedicated to weight loss, body contouring services, and holistic wellness for over 5+ years. Our team specializes in curating personalized weight loss programs utilizing scientific, non-surgical treatments with a 360-degree approach to ensure instant and sustainable results. With a strong presence in South India, VeCura has expanded to 15+ clinics and a network of 200+ wellness experts, positively impacting the lives of over 56K+ clients. We are committed to providing individualized slimming and weight loss solutions following expert consultations. VeCura Wellness is launching a premium vertical, offering a cutting-edge wellness and slimming experience for high-end clients seeking science-backed, doctor-led transformation without surgery. We are seeking a Medical Director who is passionate about preventive health, weight loss, metabolic wellness, and body aesthetics - an individual who aspires to lead rather than merely consult. Who You Are: - MBBS (required) with MD (Internal Medicine/Dermatology) - OR - MBBS + Fellowship in Obesity Medicine / Aesthetic Medicine / Lifestyle Medicine - 5-10 years of experience managing clients with obesity, PCOS, thyroid, and metabolic disorders - Enjoy creating personalized plans and collaborating with a team of dieticians, therapists, and wellness coaches - Possess an entrepreneurial mindset and are enthusiastic about establishing something from the ground up What You'll Do: - Lead the medical strategy at our Signature Lounge - Supervise IV therapy, fat-loss machines, injectables, and non-surgical protocols - Personally consult with select high-profile or complex clients - Contribute to treatment design, product formulations, and staff training - Build visibility through webinars, IG Lives, or content creation (optional but preferred) If you are a doctor ready to shape the future of wellness in India, we are eager to meet you.,

Amgen is dedicated to leveraging the power of biology and technology to combat the most challenging diseases worldwide, while enhancing the quality and longevity of people's lives. For over 40 years, Amgen has been at the forefront of the biotechnology industry, utilizing cutting-edge innovation, technology, and genetic data to expand beyond current boundaries of knowledge. As the Scientific Communications Therapeutic Area (TA) Lead at Amgen, you will be responsible for overseeing the planning, resource management, and implementation of scientific communications deliverables, including medical content and publications, for a specific disease area or key product(s) within the assigned Therapeutic Area. Reporting directly to the Scientific Communications Head in India, you will collaborate closely with global and US scientific communication and medical leads to drive the tactical planning and execution of comprehensive scientific communication plans that align with overall product strategies. In addition, you will work in collaboration with Global and US/Regional Medical planning teams, Scientific Communication Operations team, and cross-functional capability teams to ensure process alignment, standardization, continuous improvement, and innovation, incorporating digital and multi-channel approaches. Your role will involve leading high-performing and engaged teams to exceed expectations. Responsibilities include leading the Scientific Communication team in Amgen India across the designated Therapeutic Area portfolio, recruiting, retaining, developing, and motivating staff, overseeing talent management and succession planning, fostering the Amgen culture, allocating resources effectively to meet product strategy/planning needs, ensuring compliance with relevant SOPs and processes, developing and monitoring Key Performance Indicators (KPIs), and collaborating with various internal teams to support training programs and the evolution of scientific communication processes. To qualify for this role, you must possess an advanced scientific degree (Doctorate degree/Master's/Bachelor's in Science) with at least 18-23 years of experience in the Pharma Industry. You should also have 4 years of experience in Global Publication, Medical Communications, Medical Value and Access, or Medical Strategy, along with 4 years of managerial experience directly managing people or leading teams, projects, programs, or resource allocation. Preferred qualifications include an understanding of the pharmaceutical commercialization process, knowledge of regulatory and legal guidelines affecting prescription product promotion, experience with multi-channel scientific platforms, proficiency in scientific and clinical data analysis and communication, familiarity with publication guidelines and transparency standards, and a track record of strategic execution in a matrix environment. Additionally, soft skills such as strong communication, ability to work effectively in global teams, initiative, self-motivation, project management, and adaptability will be beneficial for this role. Amgen is committed to providing reasonable accommodations for individuals with disabilities during the job application process, interviews, essential job functions, and other employment-related privileges. Please reach out to us to request any necessary accommodations.,

Join Amgen's Mission to Serve Patients If you feel like you're part of something bigger, it's because you are. At Amgen, our shared mission to serve patients drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together, researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It's time for a career you can be proud of. What You Will Do The Scientific Communications Senior Manager is accountable for planning and delivering innovative scientific and medical content aligned to their designated Therapeutic Area/product (General Medicine, Inflammation, Oncology, Rare Disease, or Obesity), tailored to specific audiences globally via impactful formats and relevant channels. Reporting to a Scientific Communications Therapeutic Area (TA) Lead in India, this leader manages a small team of scientific communication team members and drives the execution of tactical Scientific Communication plans for US and global regions to deliver our Medical and overall product strategies. The Scientific Communications Senior Manager may directly partner with US/Regional Medical planning team and Scientific Communication Operations team members to drive process alignment, standardization, and adoption of innovation and transformational change. This role is responsible for creating and leading high-performing and engaged teams to exceed expectations. Roles And Responsibilities - Develop and deliver high-quality, accurate, and innovative scientific and medical content (DSE/digital/MSL materials/FAQs/Medical Information Letters) tailored to specific audiences in the US and globally via impactful formats and relevant channels. - Publication-related deliverables (manuscripts/abstracts/posters/Oral presentations, enhanced content). - Addressing Medical Information inquiries/issues. - Maintain strong partnerships with Scientific Communication Operations team in support of standardization of processes, optimizing systems, and furthering continuous improvement and innovation, including the use of digital and multi-channel approaches, as well as definition of impactful KPIs. - Drive the execution of a comprehensive scientific communication plan that shifts based on changes in the disease area and treatment landscape and in-depth awareness of insights across local affiliates and cross-functional partners. - Ensure compliance with relevant Amgen enterprise and Functional SOP(s) and system(s). - Assist in recruiting, onboarding, and training of staff members. - Support prioritization process, prepare and oversee team assignments to meet program goals on time and within budget. - Develop, maintain, cultivate, and influence strong relationships with cross-functional colleagues. - Foster Amgen culture and motivate high-performing and empowered staff. What We Expect Of You We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications - Doctorate degree with a minimum of 10 years of experience in Global Publication, Medical Communications, Medical Value and Access, or Medical Strategy. - Masters degree with a minimum of 12 years of experience. - Bachelors degree with a minimum of 14 years of experience. - Minimum of 5 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Must-Have Skills - MD, PharmD, PhD, or DO with 4 or more years of expertise in clinical research, patient care, Clinical Development, Medical/Scientific Affairs, and/or basic research (other doctorate degrees may be considered). - Prior experience in Medical/Scientific Affairs or Clinical Development within the biopharmaceutical industry, and/or clinical or research in the therapeutic area. - An understanding of the pharmaceutical commercialization process and knowledge of the regulatory and legal guidelines affecting promotion of prescription products. - Experience in publication planning, publications guidelines, and transparency standards (e.g., ICMJE, current Good Publication Practice (GPP) Guidelines). - Understanding of Amgen focused disease area and landscape and clinical data to enable critical analysis of scientific literature and communicate implications cross-functionally. - Demonstrated track record of strategic execution in a matrix environment with limited supervision. - The ability to work in teams and interface in a dynamic environment across corporate functions. Preferred Skills - Knowledge of emerging technologies in medical communications (e.g., AI tools, omnichannel engagement platforms). - Strong computer and database skills, particularly with Microsoft Office products. Soft Skills - Strong verbal and written communication skills. - Ability to work effectively with global, virtual teams. - High degree of initiative and self-motivation. - Ability to manage multiple priorities successfully. - Collaborative mindset with a strong sense of accountability and ownership. - Ability to drive continuous improvement and adapt quickly in a fast-evolving environment. - Strong project management with the ability for self-direction. What You Can Expect Of Us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination. Objects in your future are closer than they appear. Join us. EQUAL OPPORTUNITY STATEMENT We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.,

The Medical Expert in TCO (Translational Clinical Oncology) serves as the medical leader for assigned global, roll-over, and long-term follow-up studies, as well as studies in the close-out phase. Additionally, they may provide medical co-leadership for assigned aspects of global, active TCO studies under the guidance of a Clinical Program Leader (CPL). TCO, a department under the Biomedical Research division, is responsible for designing and conducting early-phase clinical studies in cancer patients, acting as a connection between drug discovery and late-phase clinical development to deliver innovative medicines for oncology conditions. Responsibilities include providing medical support to the CPL, contributing to clinical sections of protocols, Informed Consents, publications, regulatory documents, and reviewing clinical trial data. The Medical Expert may also oversee program safety reporting, represent the CPL at project team meetings and Investigator teleconferences, and lead the review of TCO submission documents. Furthermore, they are responsible for managing close-out, roll-over, and long-term follow-up studies, ensuring the quality of clinical study reports, and engaging with stakeholders internally and externally. The Medical Expert mentors junior team members, maintains expertise in regulations and procedures, and advocates for continuous improvement of quality. Key performance indicators include managing studies within timelines and regulatory standards, demonstrating strong scientific writing skills, providing quality medical review of trial data, contributing to department objectives, and receiving positive feedback from stakeholders. The role requires adherence to Novartis Values and Behaviors. Minimum Requirements: - MD or equivalent medical degree with clinical training and certification - At least 5 years of pharmaceutical industry experience - At least 2 years of clinical practice experience - Experience in hematology/oncology preferred - Knowledge of GCP and oncology clinical trials - Strong project management, communication, and interpersonal skills - Ability to work independently and in a team, adapt to changing environments, and network effectively Skills: - Clinical Monitoring - Clinical Research - Clinical Trial Protocol - Decision Making Skills - Drug Development - Health Sciences - Life sciences - Medical Strategy - Regulatory Compliance Language: - English Novartis offers a collaborative environment where passionate individuals can work together to achieve breakthroughs that positively impact patients" lives. For those interested in joining the Novartis Network, opportunities can be explored through the talent community to stay connected with suitable career options. Additionally, Novartis provides benefits and rewards to support personal and professional growth. Novartis is dedicated to fostering an inclusive work environment that represents the diversity of the patients and communities served. Accommodations for individuals with disabilities are available upon request to ensure equal opportunities during the recruitment process or job performance.,

As a Therapy Lead in our Medical Affairs function, you'll be at the forefront of shaping and executing the medical strategy and scientific engagement activities for your assigned therapeutic area or region. You'll oversee the delivery of crucial scientific support to our marketing and brand management teams, cultivate strong relationships with Key Opinion Leaders (KOLs), and champion impactful medico-marketing initiatives. This pivotal leadership role requires you to align medical strategy with business goals, all while ensuring medico-marketing activities support product promotion in line with ethical practices. Key Responsibilities Leadership & Strategic Oversight : Provide strategic direction and leadership for the medical affairs activities within your assigned therapeutic area or region. Scientific Support for Marketing & Brand Management : Offer robust scientific support, insights, and guidance to commercial teams, ensuring accuracy and scientific integrity in promotional materials and strategies. KOL Engagement & Scientific Relationship Building : Develop and nurture strong, collaborative relationships with Key Opinion Leaders and other scientific experts to foster scientific exchange and gather insights. Medico-Marketing & Scientific Communication : Drive the development and execution of medico-marketing initiatives and scientific communication plans, including publications, presentations, and educational programs. Clinical Research & Real-World Evidence (RWE) Generation : Contribute to the design and interpretation of clinical research and real-world evidence generation activities to support product value propositions. Regulatory & Compliance Leadership : Ensure all medical affairs activities adhere to relevant regulatory guidelines, industry codes, and ethical standards. Key Qualifications Education: MD, MBBS is required. An MBA or additional management qualifications will be an advantage. Experience: 7 - 10 years of experience in Medical Affairs , with at least 5 years in a leadership role . Extensive experience in providing scientific support to commercial functions , leading medico-marketing activities , and managing KOL relationships . Proven track record of developing and implementing medical strategies aligned with business objectives in the pharmaceutical industry . Therapeutic Area Expertise : Prior experience in managing medical affairs in key therapeutic areas such as Dermatology, Endocrinology, Cardiology, Gastroenterology , etc.