Jobs at Worldwide Clinical Trials

Administer and support the electronic Quality Management System (eQMS): manage user accounts, roles, permissions, and access workflows; ensure GxP compliance, data integrity, and audit readiness; assist document migration to eQMS binders; provide SME support during audits and user support for system use.

Lead Quality Assurance activities across global studies, ensuring compliance with regulations. Provide GCP consultancy and manage quality issues. Participate in risk management and audits.

Lead and oversee site contracting for clinical studies across Europe: act as SME for clinical trial agreements, negotiate contracts and budgets with sponsors and sites, supervise and mentor Site Contracts Specialists, manage contract documentation in Study SharePoint, and deliver departmental training.