Oversee high-level plans and progress of MA&EG Indication & Pipeline teams from early development through commercialization.
Partner with the MA&EG Indication & Pipeline Lead and Functional Leads and Subject Matter Experts (SME).
Drive strategic alignment, integrated medical planning, cross‑functional connectivity, governance clarity and operational excellence across MA&EG.
Coordinate and facilitate MA&EG Indication Meetings including in person meetings as needed.
Develop agendas, capture action items, distribute minutes, and ensure timely follow up across stakeholders.
Maintain organized team communication channels and ensure consistent dissemination of relevant materials.
Build and manage project timelines, trackers, dashboards, and documentation to ensure visibility and timely execution.
Manage operational oversight for IEGPs and other strategic medical plans to ensure delivery of MA&EG Asset and Indication objectives, goals, strategies, measures (OGSM).

Advanced degree (Master or PhD) in health-related discipline or equal by experience.
At least 5 years of project management experience in distinct phases of development, in different disease areas, preferably post approval phase, phase 4 and real world evidence studies.
At least 5 years of Program Management experience in a Pharmaceutical or Biotech environment, preferably cross-cultural and on global project teams.
Strong project management skills; broad exposure to Medical Affairs process; advanced planning experience with Project Management Tools. PMP (Project Management Professional) certification is an advantage.
Strong verbal and written English communication skills (English primary fluency or full professional proficiency).

Project Manager – Medical Affairs, Evidence Generation

Key skills