Role & responsibilities

- Job Family: Medical &
- Scientific Affairs

- Division: EPD Established Pharma

- Nature of Role: Non-sales, field-based scientific support and stakeholder engagement.

Key Responsibilities

- Clinical Research &
- Trials:

Direct and oversee phase III &
- IV human clinical trials, contribute to clinical protocols, and monitor adherence.

- Investigator Management: Recruit clinical investigators, negotiate study designs and costs, and oversee investigator-initiated studies.

- Stakeholder Engagement: Build and maintain relationships with Key Opinion Leaders (KOLs), healthcare professionals (physicians, nurses, pharmacists), and medical societies.

- Safety &

- Compliance:

Participate in adverse event reporting, monitor safety responsibilities, and ensure alignment with regulatory guidelines.





- Cross-Functional Support: Collaborate with marketing, sales, and pharmacovigilance teams to deliver scientific presentations and medical projects.

Qualifications &

- Skills

- Education: Graduate or Post-Graduate Medical Degree (MBBS/MD) or degrees in Pharmacology/Allied Sciences.

- Experience: Experience working in medical affairs within the pharmaceutical or healthcare environment.

- Core Skills: Solid scientific acumen, excellent communication and presentation skills, and familiarity with clinical trial regulations.

Preferred candidate profile

MD PHARMACOLOGY

📌 Regional Medical Advisor - Delhi/Kolkata
🏢 FUTUERA
📍 Delhi