Global Pharma is looking for a contract Global Clinical Trial Manager, responsible for managing European and/or global clinical trial activities across Phases I–III within the Cell Therapy area.

Key Responsibilities

The role involves managing the European component of global outsourced clinical trials while overseeing CROs and external vendors to ensure quality and
timely delivery. Responsibilities include developing and reviewing key study documents such as protocols, informed consent forms, case report forms, and clinical study reports, as well as maintaining study timelines and contributing to study budgets. The position supports RFP development and vendor selection, coordinates data review and reporting activities, and ensures effective management of site budgets and contracts. The Clinical Trial Manager acts as the primary point of contact for CROs, resolving study-related issues, and collaborates closely with cross-functional teams to drive trial progression. Oversight monitoring visits may be required, along with involvement in study
Logistics, planning, and execution.

Requirements

Candidates should have experience in multinational clinical trials, ideally within Europe, and
demonstrate a strong understanding of ICH-GCP, FDA, and EU regulatory requirements. Experience managing CROs and vendors is essential, with monitoring experience considered advantageous. A background in oncology or cell therapy is preferred. Strong organisational, communication, and problem-solving skills are
required, along with the ability to manage multiple priorities and work independently.