Position

Global Development Associate Medical Director (Job ID R- )

Location

Barcelona, Spain – 3 days a week on‑site commitment.

Responsibilities

• Ensure the risk‑benefit of clinical studies, maintaining the highest ethical and safety standards in compliance with FDA, EMEA, ICH, GCP guidelines and AZ SOPs.
• Work cross‑functionally in the design and implementation of clinical hemato‑oncology projects with the Clinical Sub‑Team (CST).
• Contribute to the development of program strategy for assigned compounds/programs and collaborate on business cases for governance approval.
• Provide clinical input to influence study design in collaboration with investigators, key external experts, study sites and internal stakeholders.
• Participate or lead review and assessment of new opportunities and ESRs as needed.
• Support interactions with global medical affairs, marketing, and commercial teams to ensure cros...