Regional Medical Advisor
MSD
Full time- 3+ years
- Not Disclosed
- Kolkata, India
- Post Date: Apr 03, 2024
- End Date: Jun 03, 2024
- 3+ years
- Not Disclosed
- Kolkata, India
- Post Date:Apr 03, 2024
- End Date: Jun 03, 2024
Skills:
- pharma
- clinical research
- MD
Job Description:
Responsibilities
- Scientific Expertise Developing and maintaining an in-depth understanding of the company's products, therapeutic areas, and relevant scientific research. Staying updated on the latest medical and scientific advancements, clinical guidelines, and treatment protocols.
- SL & KDM Engagement Building and maintaining relationships with Scientific Leaders (SLs), Key decision makers (KDMs) healthcare professionals, and academic institutions. Engaging in scientific discussions, presenting clinical data, and providing educational support to KOLs regarding the company's products and therapeutic areas.
- Support to medical strategy In alignment with the line manager, provide strategic inputs, and expertise, to product management towards ethical promotion of assigned products
- Medical Education Providing scientific and medical education to internal stakeholders, including sales teams, marketing teams, and other cross-functional colleagues. Collaborating with the Medical Affairs team to develop and deliver training materials, presentations, and scientific symposia.
- Scientific Exchange Facilitating scientific exchange and knowledge transfer between the company and external stakeholders. Participating in medical conferences, advisory boards, and scientific meetings to gather insights, share data, and contribute to the scientific community.
- Clinical Data Communication Interpreting and communicating clinical trial data, real-world evidence, and other scientific information to healthcare professionals, regulators, and other relevant stakeholders. Ensuring accurate and compliant dissemination of scientific information in accordance with regulations and company policies.
- Clinical Research Provide medical support for local studies, including need-based visits to identify study sites Lead Investigator Initiated Trials
- Cross-functional Collaboration Collaborating closely with cross-functional teams, including Clinical Development, Regulatory Affairs, Marketing, and Market Access, to provide scientific input, support clinical trial design, contribute to regulatory strategies, and align on medical communication plans.
- Facilitate access to scientific leaders as appropriate.
- Support as well as own medical initiated projects in line with therapy area that would involve a strong stakeholder interface
- Provide scientific support to sales team
- Medical Information Addressing medical inquiries and providing timely and accurate responses to healthcare professionals, patients, and other stakeholders. Ensuring that medical information materials, such as medical letters and FAQs, are up to date and compliant.
- Sales Force Training Provide medical training to sales colleagues on the therapy areas assigned Assist in pre-launch and launch training to sales staff for new products.
- Compliance Adhering to relevant legal, regulatory, and compliance guidelines, including the organization's code of conduct and industry-specific regulations. Ensuring all activities and interactions are conducted ethically and in compliance with applicable laws and regulations.
- Overall, RMA in Medical Affairs acts as a scientific expert and liaison between the company and external stakeholders, playing a crucial role in building scientific credibility, fostering relationships, and supporting the company's strategic objectives in the healthcare industry.
Qualfication & Expereience
- Educational Background A strong academic background in life sciences, such as a medical degree (MD), doctorate (Ph.D.), or pharmacy degree (Pharm.D.). Other relevant degrees in biology, pharmacology, or related fields may also be considered.
- Industry Experience Prior experience in the pharmaceutical, biotechnology, or medical device industry is often preferred. This could include experience in clinical research, medical affairs, or related roles that have exposed the candidate to scientific and medical aspects of the industry.
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