Define and drive the clinical strategy for the assigned care area (molecular imaging).
Lead the development of Target Product Profiles (TPPs), Integrated Evidence Generation Plans (IEGPs), and clinical development plans.
Represent the therapeutic area in governance forums and regulatory interactions.
Engage with KOLs and external experts to shape development strategy.
Oversee cross-functional alignment across Regulatory, Medical Affairs, Commercial, and Clinical Operations.
Mentor and guide clinical scientists and medical monitors working within the care area.
Provide medical oversight for one or more clinical trials.
Review safety data, assess adverse events, and support dose modifications or protocol amendments.
Respond to investigator queries and support site engagement.
Participate in Data Safety Monitoring Boards (DSMBs) and internal safety reviews.
Contribute to clinical study reports (CSRs), regulatory submissions, and medical writing.
Collaborate with Clinical Operations and Pharmacovigilance teams.
MD or PhD with deep expertise in the therapeutic area.
Extensive experience in clinical development.
Strong strategic thinking and leadership capabilities.
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We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.
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Relocation Assistance Provided: No