Clinical Project Manager

Job not on LinkedIn

🕒 September 5, 2025

⚔️ Virginia – Remote

⚔️ Virginia – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥 Clinical Operations

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Beaufort

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🚀 Aerospace

🎖️ Defense

🏭 Manufacturing

🔥 Funding within the last year

💰 Private equity on 2025-10

Aerospace • Defense • Manufacturing

Beaufort is a trusted leader in aerospace and defence manufacturing focused on survival and force-protection technologies. Part of the Survitec Group, Beaufort develops and supplies life-saving equipment and capability enhancements that protect military personnel, redefining performance, capability and comfort for force protection. The company emphasizes industry-leading technology, expertise and excellence to safeguard lives for military customers worldwide.

📋 Description

• 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. • 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. • Monitor and reconcile project budgets. • Collaborate with finance teams to provide accurate forecasts and manage scope creep. • Provide oversight and guidance to CRAs regarding monitoring activities, site management, and issue resolution. • Review and/or contribute to key study documents such as protocols, CRFs, monitoring plans, site manuals, and data management plans.

🎯 Requirements

• Bachelor’s degree in biological sciences, pharmacy, nursing, or a related health discipline required; advanced degree preferred. • Minimum of 5 years’ experience in clinical research with at least 3 years in a project management role. • Proven history of leading complex global or domestic clinical trials within a CRO or sponsor environment. • Experience managing clinical studies in in vitro diagnostics (IVD) and Medical Device. • Applied deep knowledge of ICH-GCP and global regulatory requirements to ensure compliance across all phases of clinical trial execution.

🏖️ Benefits

• Highly competitive compensation and benefits package