Teams at Parexel

Coordinates clinical-study sourcing for depots, investigational medicinal products, couriers, medical devices, and ancillary supplies. Responsibilities include supplier research and evaluation, quotations, purchase requests, contracting, import/export documentation, returns, quality issue resolution, risk mitigation, sourcing ticket management, and supply planning. The role advises internal stakeholders, analyzes sourcing data, supports compliant procurement, manages supplier relationships, and mentors junior team members in a remote, fast-paced clinical research environment.

Supports global pharmaceutical labeling operations, including regulatory-compliant document development, artwork and change-management coordination, regulatory tracking, regional implementation, version control, SOP maintenance, and stakeholder training. The role ensures labeling governance and compliance across the product lifecycle while collaborating with regulatory, operations, artwork, and regional teams.

Manages global clinical trial operations from protocol design through study closeout, including CRO and vendor oversight, regulatory tracking, recruitment, budgets, timelines, risk mitigation, trial documentation, training, and stakeholder coordination. Supports inspection readiness, process improvement, team onboarding, and operational strategy across Phase I-IV studies.