Medical Director (Project Management)

Description:

The Medical Science Director Oncology will serve as an internal scientific expert supporting Oncology, Biosimilars, Branded Oncology and GRx Injectable products. This role has responsibility for responding to Medical Information Requests, clinical support for the field sales teams, clinical support for customers and the product development strategy. This positiong will report to the VP- Medical Affairs

Essential Functions:

• Provide clinical and scientific expertise in oncology to support internal teams, healthcare professionals (HCPs), and stakeholders. Respond to medical information requests from healthcare providers, external partners, and internal departments with accurate, balanced, and timely information
• Lead and participate in advisory boards, KOL engagements, and scientific exchange to gather and provide insights for product development and medical strategy. Collaborate with Clinical Operations to provide medical oversight and support for clinical trials including investigator-initiated studies. Work closely with cross-functional teams (R&D, clinical development, regulatory affairs, commercial) to ensure medical insights are integrated into company strategies and product life cycle management.
• Develop and deliver high-quality scientific presentations and materials for both internal and external audiences, including HCPs and key opinion leaders (KOLs).
• Ensure that all medical communication, promotional material reviews, and activities comply with regulatory requirements, company policies, and ethical standards.
• Provide ongoing medical and scientific training to internal teams, including sales and medical affairs, to ensure a deep understanding of oncology products and disease states.

 

Education:

• Ph. D. Clinical or Scientific discipline - Required

Experience:

• 7 years or more in Experience in the clinical, pharmacy, pharmaceutical or biotechnology industry Specifically in the oncology therapeutic area
• Just underneath that, add “5 years or more” and Strong clinical background in oncology, with a deep understanding of cancer treatments, therapeutics and clinical practice  - Required
• 5 years or more in Proven experience in medical communications, including responding to medical information requests and delivering scientific content.

Skills:

• Executive presence and ability to manage changes in business priorities. - Advanced
• Able to work well under pressure and in appreciation of pre-defined and often aggressive timelines. - Advanced
• Excellent written, organizational and verbal communication skills with the ability to present complex information to both scientific and non-scientific audiences. - Advanced
• Computer literate with MS Office products including PowerPoint, Word, and Excel. - Advanced
• Knowledge of pharmaceutical regulatory requirements (FDA, EMA, etc.) and industry guidelines. - Advanced
• Strong organizational, project management, and leadership skills. - Advanced
• Experience working closely with clinical development and medical affairs teams. - Advanced
• Established relationships with KOLs and key stakeholders in the medical community - Advanced
• Previous experience in regulatory submissions or product launch activities - Advanced

 

Amneal is an Equal Opportunity Employer that does not discriminate on the basis of sex, age, race, color, creed, religion, national origin, sexual orientation, gender identity, genetic information, disability, veteran status, liability for service in the U.S. Armed Forces or any other characteristic protected by applicable federal, state, or local laws.