Clinical Project Manager

About this role

Beaufort seeks a skilled Clinical Project Manager (CPM) to work alongside a top-notch team of clinical researchers. We participate in an exciting and growing industry and that growth fuels the need to continue to build our team and support our mission.

This is a unique opportunity to join a growing CRO where your leadership will directly impact trial success and client satisfaction.

Position Summary

The Clinical Project Manager (CPM) leads the end-to-end delivery of clinical trials across diverse therapeutic areas, ensuring strategic alignment, operational excellence, and regulatory compliance. This role serves as a cross-functional leader and primary liaison between sponsors, vendors, and internal teams to drive successful trial outcomes.

Key Responsibilities

Clinical Trial Oversight & Leadership

• Provide strategic and operational oversight for assigned clinical studies from start-up through close-out.
• Lead the cross-functional project team (e.g., clinical operations, data management, statistics, safety, and medical writing) to meet or exceed project goals.
• Act as primary contact for Sponsors and serve as a Subject Matter Expert (SME) for designated clinical programs.
• Ensure compliance with ICH-GCP, SOPs, protocols, and regulatory requirements.

Project Management

• Create, manage, and maintain detailed project plans including timelines, deliverables, KPIs, and milestones.
• Track project performance using appropriate systems, tools, and techniques (e.g., project dashboards, risk logs, scope change trackers).
• Identify project risks and develop proactive mitigation strategies in collaboration with sponsors and internal stakeholders.
• Implement structured change control processes to manage protocol amendments or scope changes.
• Lead regular internal and sponsor-facing status meetings, ensuring clear communication of project progress, challenges, and action items.

Project Financial Management

• Monitor and reconcile proj...