Assistant Manager - Medical Affairs

GUFIC BIOSCIENCES LIMITED; Mumbai; On-site; INR 1,500,000 - 2,200,000; Full time

Job summary

GUFIC BIOSCIENCES LIMITED is seeking a Medical Affairs professional to support coordination, medical information, and publications across neurocare products. The role involves training the field force, handling scientific queries, and disseminating evidence-based content.

Responsibilities include literature reviews, external representation at conferences, CMEs, and field visits across India to gather insights and strengthen physician relations. A strong medical background is essential.

Responsibilities

• Collaborate with the Neuro team and other cross-functional departments for the management of strategic initiatives.
• Create and update product monographs, training slide decks, and CME slide decks for the botulinum toxin portfolio.
• Conduct induction and refresher medical training for the field force to communicate complex clinical information to healthcare professionals.
• Manage and resolve scientific queries from the field force regarding product use, efficacy, and safety.
• Conduct in-depth literature searches to support medical communications, product positioning, and new product evaluations.
• Provide continuous medical support for existing brands, ensuring content is evidence-based and up-to-date.
• Publish manuscripts and review articles in peer-reviewed journals to strengthen the organization's scientific reputation in neurocare.
• Attend and represent the organization at key conferences, workshops, and divisional meetings.
• Coordinate CMEs and webinars to facilitate scientific exchange with KOLs.
• Conduct field visits PAN India with the sales team to gather medical insights and strengthen doctor relationships.
• Evaluate new product/molecule opportunities with mechanism of action, clinical data, and competitive landscape; provide Go/No-Go recommendations.

Job description

1.Coordination & Collaboration:

• - Collaborate with the Neuro team and other cross-functional departments for the management of strategic initiatives.

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 new 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.