About the Role

We are seeking an experienced Clinical Project Manager (CPM) to lead the delivery of global and regional clinical studies for a growing portfolio of biotech and pharmaceutical clients. This position offers the opportunity to work within a dynamic CRO environment, managing studies across multiple therapeutic areas while acting as the primary point of contact for sponsors.

The ideal candidate will have a strong CRO background, previous CRA experience, and a proven track record of managing complex clinical trials, client relationships, budgets, and cross-functional teams.

Key Responsibilities

• Lead and oversee the operational delivery of clinical trials from start-up through close-out.
• Serve as the primary contact for sponsors, ensuring exceptional client management and communication.
• Manage project timelines, budgets, resources, risks, and deliverables.
• Coordinate cross-functional teams including Clinical Operations, Regulatory, Data Management, Medical Monitoring, and Vendors.
• Drive study performance through proactive issue identification and mitigation.
• Conduct project meetings, governance reviews, and sponsor updates.
• Support business development activities, including participation in bid defense meetings and proposal development where required.
• Review project financials and contribute to budget management and forecasting.
• Ensure studies are conducted in compliance with ICH-GCP, company SOPs, and applicable regulations.
• Build strong relationships with both internal stakeholders and external clients, particularly within the biotech sector.