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ile meeting as needed.
Initiate and direct the conduct of Advisory Board meeting under category medical strategic needs.
Initiate global and local expanded access programs as needed
Be consulted and provide guidance in responding unsolicited scientific queries from external healthcare professionals, in conjunction with the medical information function.
Review and approve promotional materials, speaker slides to ensure scientific accuracy and compliance with Pfizer policies and local regulations.
Support Regulatory Affairs for product labeling review.
Risk Management Plan (RMP):
Represent Country RMP author for the responsible products.
Provide medical inputs to local RMP core team.
Lead and delivery required material and/or action which shall implement by Medical.
Identify, build and leverage scientific relationships with key opinion leaders in relevant medical category.
Other medical affairs projects appointed by supervisor.
People Manager Responsibilities:
Leading the performance of the Field medical (MSL, Medical Managers ) team by setting business objectives and priorities that ensure delivery of the Medical Affairs plans and metrics.
Developing the MSL team's capabilities to achieve excellence in scientific engagement through management and coaching of their people.
Planning and prioritizing MSL resources and activities to deliver value externally with external experts, and internally with matrix partners to support business objectives
REQUIRED SKILL SET
• Technical
Champion and role model of medical professionalism
Strategic and innovative thinking and demonstrates business acumen
Proficiency in oral and written English
Excellent presentation skills
Concern for quality and timeliness
Strong communication and influence skills
• Education
Graduate degree in Medicine with specialization, or appropriate higher degree PhD, PharmD experience in medical sciences
Degree in advanced sciences or post-graduate degree courses preferred.
• Experience
Minimum 5-year experience in the pharmaceutical industry with expertise in clinical research and medical affairs
Comprehensive knowledge of drug clinical development process, policies and regulations
People Management Experience
Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
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