Global Associate Director Medical Affairs; GADMA), Oncology-Gynecological Malignancies

Role Summary

The Global Associate Director Medical Affairs (GADMA) has scientific and working knowledge in their area of responsibility (e.g., defined tumor, asset, vaccine) and is responsible for supporting execution of the Global Medical and Scientific Affairs (GMSA) portion for their assigned Therapeutic Areas (TA) or across areas as needed, in alignment with the Global Value & Implementation (V&I) Plans. They support the global cross-functional teams, engage with their network of scientific leaders and bring executional excellence and business savviness to the organization.

They have a focus on the US, while also supporting the Rest of the World (ROW). The GADMA works as part of a high-performing and results-driven team.

• Supports execution of the annual V&I plan with medical affairs colleagues and acts as an empowered partner, making informed decisions with a strategic and agile mindset.
• Partners with the GDMA in executing global medical affairs team meetings and related tactics.
• Supports the global medical affairs team to ensure execution of agreed medical tactics and leverage best practices.
• With direction from the EDMA and/or GDMA, partners with global Commercial, global Outcomes Research, global Policy and global Market Access to inform and support the development and execution of V&I plans.
• Consolidates actionable medical insights from countries and regions.
• Organizes global expert input events (advisory boards and expert input forums) to answer Our Company’s questions about how to develop and implement new medicines or vaccines.
• Organizes global symposia and educational meetings.
• Supports the GDMA in identifying and communicating global and regional content and training requirements.
• Engages with a network of international scientific leaders and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies) about Our Company’s emerging science, building an important network and partnership internally and externally. Monitors external changing environment in partnership with the competitive intelligence (CI) team.
• Manages programs (patient support, educational or risk management) to support appropriate and safe utilization of Our Company medicines or vaccines.
• Demonstrates and champions Ways of Working, emphasizing innovation, medical modernization, defining team priorities, and focusing on the impact to the patient.
• Manages assigned budget with strong financial stewardship.
• Participates in Investigator-Initiated Study proposals reviews in collaboration and guided by EDMA or GDMA.

• MD, PhD or Pharm
  
  D and recognized medical expertise.
• 2+ years pharmaceutical (or related) industry experience in the affiliate arena.
• Strong prioritization and decision-making skills.
• Able to effectively collaborate with partners across divisions in a matrix environment.
• Excellent interpersonal, analytical, communication (written as well as oral) skills, in addition to results-oriented project management skills.

• Scientific leadership and other key stakeholders (payers, public groups, government officials, medical professional organizations) in the assigned therapeutic area.

#eligibleforERP

Accountability, Biostatistics, Budget Management, Clinical Data Management, Clinical Medicine, Clinical Research, Clinical Trial Management, Decision Making, Ethical Compliance, Evidence-Based Medicine, Global Market, Global Policy, Good Clinical Practice (GCP), Innovation, Leadership, Medical Affairs, Oncology Marketing, Partnership Development, Patient Recruitment, Patient Safety, Pharmacovigilance, Project Management

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US and Puerto Rico Residents Only

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