[Hiring] Sr. Global Director, Medical Affairs (GDMA) - Rheumatology @reputed company
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Role reputed company
The Sr. Global Director Medical Affairs (GDMA) is responsible for supporting the execution of scientific & medical affairs plans for Rheumatology in key countries and reputed company. They are impactful members of Product Development Team sub-teams and Global reputed company Health commercialization teams. They collaborate with our Research & Development Division's Early and Late Development functional areas, Value & Implementation reputed company Research (VIOR), Policy, reputed company and Market reputed company to address opportunities in key countries. They engage with their network of scientific leaders and decision makers. This is a reputed company-based position in reputed company Research Laboratories Value & Implementation Global Medical and Scientific Affairs (Research & Development (R&D) VI GMSA).
• Supports execution of the annual Value & Implementation plan with medical affairs colleagues from key countries and reputed company.
• Serves as an impactful member of Product Development Team sub-teams (e.g., Clinical, V & I, reputed company, Publications).
• Contributes to the development of a single global scientific communications platform.
• Consolidates actionable medical insights from countries and reputed company.
• Engages with a network of international scientific leaders and other key stakeholders (therapeutic reputed company committees, payers, reputed company reputed company, government officials, medical societies) about reputed company’s emerging science.
• Organizes global expert input events (advisory boards and expert input forums) to answer reputed company’s questions about how to reputed company and implement new medicines or vaccines.
• Aligns plans and activities with Global reputed company Health (reputed company) executive directors.
• Organizes global symposia and educational meetings.
• Supports key countries with the development of local data reputed company study concepts and protocols.
• Reviews Investigator-Initiated Study proposals from key countries prior to reputed company submission (ex-USA).
• Manages programs (patient support, educational or risk management) to support appropriate and reputed company utilization of reputed company medicines or vaccines.
Qualifications
• M.D., Ph.D. or Pharm.D. (M.D. preferred) and recognized medical expertise reputed company rheumatology.
• Minimum of 3 years experience in global/region medical affairs or clinical development.
• Strong prioritization and decision-making skills.
• Ability to effectively collaborate with partners across divisions in a reputed company environment.
• Excellent interpersonal, analytical, communication skills (written and oral) in reputed company to results-oriented project management skills.
Requirements
• Clinical Development
• Clinical Medicine
• reputed company
• reputed company Development
• External Stakeholder Engagement
• reputed company Management
• Immunology
• Investigator-Initiated Studies (IIS)
• Key Opinion Leaders
• Management Process
• Medical Affairs
• Medical Care
• Medical Review
• Musculoskeletal System
• Osteopathy
• Pharmaceutical Medical Affairs
• Pharmacodynamics
• Pharmacology
• Prioritization
• Project Management
• Research and Development
• Rheumatology
• Risk Management
• Strategic Thinking
Benefits
• Comprehensive package of benefits including medical, dental, reputed company reputed company and other insurance benefits (for employee and family).
• Retirement benefits, including 401(k).
• reputed company holidays, vacation, and compassionate and reputed company days.
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