Senior Regional Medical Affairs Manager
4 days ago
**Job**:
- Development and management of plans in collaboration with the respective teams in the Asia Region
- Implement medical strategies and programs for the company’s products in Asia
**Duties**:
- Develop and execute medical strategies supporting both innovation pipeline and life-cycle management activation initiatives
- Ensure deployment and compliance with medical governance policies including but not limited to promotional and non-promotional interactions with HCPs/HCOs, copy material review/approval & medical information inquiry management
- Ensure adequate medical support for interaction with external regulatory bodies
- Ensure adequate regional KOLs scouting, mapping, and engagement in the respect of the compliance, local rules, and regulations
- Delivery of scientifically accurate, objective, current, and consistent responses to unsolicited product inquiries
- Establish good networking with regional thoughts leader to perform medical educations programs and other meetings or activities involving medical experts in the region of responsibility, in collaboration with partners and HQ
- Review promotional materials developed by partners when applicable to ensure compliance and that adequate messages on the company products are delivered to the HCPs in alignment with the HQ strategy and plans
- Ensure safety signals and pharmacovigilance reports are made by the partners in compliance with the company SOP
- Support local manuscript and publications preparation in collaboration with partners or HQ, when it is applicable
- Ensure the requested support for medical information activities based on the company SOP and in collaboration with HQ
- Ensure synergies and collaboration with HQ, other Regional Senior Managers, and Commercial counterparts
**Profile**:
- Master Degree in Science, Business Administration, Ph.D., or medical education (M.D)
- 10 years of experience in the Pharmaceutical/ Healthcare Industry, in the area of medical affairs/ management
- Adequate training and experience in clinical studies and Medical Affairs
- Strong working knowledge of regulatory requirements, product development requirements and standards, regulations, and internal quality documents
- Excellent communication and fluent in English and Chinese to communicate with partners. French and German would be an asset
- Take ownership for delivering against areas of responsibility, demonstrating strong organizational skills and decision-making with a dynamic and flexible working style
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