We are hiring aGlobal Clinical Head (GCH)for Obesity/Diabetesin our Late Cardiovascular, Renal and Metabolism (CVRM)Global Development team. This is a key role where you, with your strong leadership skills and drug development experience, will impact and drive development programs in a dynamic global setting. This role reports to the Vice President, Clinical Metabolismand is based in Boston, MA or Gaithersburg, M.D.
What you99ll do:
The GCH is the most senior medical scientific authority on an asset team and is a core member of the Global Product Team (GPT). The GCH is accountable for all clinical and scientific aspects of the asset(s), including benefit/risk assessment, scientific strategies for clinical components of the Target Product Profile (TPP), Target Product Claim (TPC), Clinical Development Plan (CDP), and core labelling. The GCH develops the project strategy in partnership with the GPL/GPT. The GCH co-leads the Clinical Product Team (CPT) and has accountability for the clinical deliverables.
Accountabilities include:
- Along with the Global Product Leader, provide scientific strategies for clinical components of the TPP, TPC, CDP, and core labelling
- Accountable for the clinical parts of CPT deliverables
- Responsible for overall clinical and scientific content for the asset
- Work closely with the Clinical Operations lead and ensure the CPT rapidly implements new processes, systems and learning
- Perform medical prioritization of clinical activities within the clinical program
- Single-point accountable leader for the design, delivery and interpretation of clinical studies ensuring ethical and scientific integrity in compliance with AZ policies and Good Clinical Practice
Basic Qualifications
- Graduate of a recognized school of medicine with an M.D. degree or MBBS or equivalent, with 5+ years proven experience in drug development. Specialization in Endocrinology would be preferred.
- Demonstrated deep late-stage clinical and research expertise in Obesity and/or Type 2 DM
- Delivered multiple complex and large studies (e.g., including but not limited to international outcome studies).
- Demonstrated success in influencing global and local cross-functional stakeholders.
- Experience assessing the benefit/risk profile of an asset and creating patient risk management plans.
- Experience with global regulatory submissions and interacting with major regulatory agencies.
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. Thats why we work, on average, a minimum of three days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
As AstraZeneca continues to put patients at the forefront of our mission, we are excited for our move to Kendall Square/Cambridge in 2026.
The annual base pay for this position ranges from $331,874 to $497,810. Our positions offer eligibility for various incentivesan opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
Date Posted
17-Jun-2026
Closing Date
06-Jul-2026