1.Coordination & Collaboration:

- - Collaborate with the Neuro team and other cross-functional departments for the management of

strategic initiatives.

- - Partner with the marketing team to develop scientifically accurate promotional materials (Visual

Aids, LBLs, PILs, newsletters).

- - Collaborate with third-party agencies for outsourced medical inputs, ensuring quality and

adherence to briefs.

2. Marketing & Training Support:

- - Create and update comprehensive product monographs, training slide decks, and CME slide

decks for the botulinum toxin portfolio.

- - Conduct induction and refresher medical training for the field force, ensuring they can effectively

communicate complex clinical information to healthcare professionals (HCPs).

- - Manage and resolve scientific queries from the field force regarding product use, efficacy, and

safety.

3. Medical Information & Publications: • - Conduct in-depth literature searches to support medical communications, product positioning, and recent product evaluations. • - Provide continuous medical support for existing brands, ensuring all content is evidence-based and up-to-date. • - Publish manuscripts and review articles in peer-reviewed journals to strengthen Organizations's scientific reputation in the neurocare therapeutic area.

4. KOL Engagement & External Representation:



• - Attend and represent Organization’s at key conferences, workshops, and divisional meetings • - Coordinate for CMEs and webinars to facilitate scientific exchange with KOLs. • - Conduct field visits (PAN India) with the sales team to gather medical insights, competitive intelligence, and strengthen doctor relationships.

5. Product Evaluation & Strategic Input: • Evaluate new product/molecule opportunities through comprehensive reviews, including mechanism of action, clinical trial data, and competitive landscape analysis, providing strategic "Go/No-go" recommendations for the division.

6. Regulatory & Pharmacovigilance Support: • - Author and review domestic and export Product Package Inserts (PIs) ensuring compliance with DCGI and target country guidelines. • - Coordinate the reporting and follow-up of Adverse Events (AEs) with the QA/QC team, ensuring timely and compliant closure.

7. Clinical Trial Support: • - Provide medical support for clinical trial projects assigned to the division, ensuring documentation is accurate and timelines are met.

8. System & Process Adherence: • - Ensure all medical activities comply with internal SOPs, pharmacovigilance requirements, and industry regulations. • - Contribute to building a robust medical documentation system within the division.

📌 Assistant Manager - Medical Affairs (Mumbai)
🏢 Gufic Biosciences
📍 Mumbai