Job Description

- Senior Medical Advisor- Mumbai
The Medical Advisor will provide scientific and clinical expertise, focusing on the cardiovascular therapeutic area. This role will support the development of medical strategies, assist in the clinical development process, and engage with both internal and external stakeholders. The successful candidate will report directly to the GM - Medical Affairs and work as an individual contributor.
Key Responsibilities:

• Medical Expertise and Support:

• Provide scientific and medical support to internal teams (e.g., regulatory, marketing, and sales) on cardiovascular-related products and clinical data.
• Review and approve promotional and scientific content to ensure medical accuracy and compliance.
• Respond to medical queries from internal and external stakeholders, ensuring evidence-based and scientifically accurate information.
• Clinical Development:

• Collaborate with the clinical development team in cardiovascular trials, offering input on study design, data analysis, and interpretation.
• Assist in preparing clinical study reports, publications, and other medical documents as required.
• KOL and External Engagement:

• Build and maintain relationships with key opinion leaders (KOLs) and healthcare professionals in the cardiovascular field.
• Support the organization of scientific meetings, advisory boards, and conferences.
• Medical Strategy and Communication:

• Contribute to the development and execution of medical affairs strategies aligned with business goals.
• Provide support for regulatory submissions and ensure effective communication of clinical data.
• Training and Development:

• Conduct training sessions for internal teams, especially on the cardiovascular therapy area and product-related information.

• Share insights from scientific literature and research findings with cross-functional teams.

Qualifications:

• Education:

• MBBS and MD in Pharmacology (or equivalent medical qualifications).

• Experience:

• 2-4 years of experience in Medical Affairs, Clinical Research, or related fields in the pharmaceutical industry, particularly in the cardiovascular therapy area.
• Prior experience in interacting with KOLs and contributing to clinical trial development is highly preferred.

• As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning, execution, clinical trials/research and the data collection activities.
• Contributes to implementation of clinical protocols, and facilitates completion of final reports.
• Recruits clinical investigators and negotiates study design and costs.
• Responsible for directing human clinical trials, phases III & IV for company products under development.
• Participates in adverse event reporting and safety responsibilities monitoring.
• Coordinates and provides reporting information for reports submitted to the regulatory agencies.
• Monitors adherence to protocols and determines study completion.
• Coordinates and oversees investigator initiations and group studies.
• May participate in adverse event reporting and safety responsibilities monitoring.
• May act as consultant/liaison with other corporations when working under licensing agreements.

Skills Required