About this role

Responsible for projecting, planning, executing, and overseeing all supply chain activities related to clinical trial materials.
Manage the procurement, production, packaging, labeling, distribution, and inventory of clinical trial materials.
Ensure clinical supplies are delivered on time, within budget, and in compliance with regulatory requirements.
Follow-up communication with various departments and stakeholders.

Bachelor’s degree in supply chain or other disciplines with equivalent industry experience.
8+ years of experience in clinical or in combination with commercial supply chain management, with at least 3 years in a senior or managerial role.
In-depth knowledge of clinical trial processes, GMP, GCP, and regulatory requirements.
Proven experience in managing complex global supply chains for clinical trials (including Europe, APAC, and South America).
Proven experience with high-complexity Phase 3 trials.

Equal employment opportunities to all applicants without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, or veteran status.
Comprehensive medical and dental insurance.
Flexible work arrangements.

Associate Director, Clinical Supply

Key skills