Medical Advisor

IntelliMed Healthcare Solutions is a Medical Affairs services provider located in Mumbai. Our expertise lies in providing medical, clinical, and economic data, communication, and regulatory support to stakeholders across the healthcare continuum. We specialize in contract/outsourced Medical Affairs Services to help pharmaceuticals, medical devices, and nutraceuticals build Market Access. Our team has over 25 years of experience in medical affairs within leading Indian and multinational companies.

The Medical Advisor serves as the scientific and clinical expert for assigned therapeutic area(s) and products within a pharmaceutical company. They are responsible for providing medical and scientific support to cross-functional teams including marketing, sales, regulatory, and clinical research, ensuring medical accuracy and compliance in all company activities.

Key Responsibilities:

1. Scientific & Medical Expertise

• Act as the internal scientific expert for assigned product(s) and therapeutic area(s).
• Provide expert input on clinical development plans, investigator-initiated studies (IIS), and publication strategy.
• Interpret and communicate complex scientific data to both internal and external stakeholders.

2. Medical Strategy & Support

• Contribute to the development and execution of the medical strategy aligned with brand strategy.
• Provide scientific support in the development of promotional and educational materials ensuring medical accuracy and compliance with applicable regulations.

3. External Expert Engagement (KOL Management)

• Identify, develop, and maintain relationships with Key Opinion Leaders (KOLs), investigators, and external experts.
• Organize and participate in Advisory Boards, round-table meetings, and scientific discussions.

4. Training & Internal Support

• Deliver therapeutic area and product training to sales and marketing teams.
• Provide medical support to commercial teams for product launches, field force queries, and strategy execution.

5. Medical Information & Compliance

• Respond to medical information requests from HCPs.
• Ensure all activities are in accordance with local regulatory requirements, industry codes of practice, and internal SOPs.

6. Clinical Research & Real-World Evidence

• Collaborate on the design and execution of post-marketing clinical studies and real-world evidence (RWE) programs.
• Support local implementation of global clinical trials, including site identification and feasibility.

MBBS/MD/PhD/BDS/PharmD , or specialized related field.

2–5 years of experience is a MUST have

Key Competencies:

• Strong scientific acumen and ability to interpret and communicate data.
• Excellent interpersonal and communication skills.
• Proven ability to work cross-functionally.
• Strong understanding of local regulatory and compliance frameworks.
• Strategic thinking and customer focus.