Remote Clinical Project Manager – Inflammation (US-Only)

Syneos Health/ inVentiv Health Commercial LLC; South Carolina; Remote; USD 110,000 - 160,000; Full time

Benefits offered by this job

Company car

Health benefits

401k plan

Stock purchase plan

Flexible PTO

Job summary

Syneos Health is seeking an Experienced Clinical Project Manager for inflammation studies. This remote-US role requires ownership of end-to-end trial execution, strong leadership of cross-functional teams, and hands-on oversight of vendors and CROs in a sponsor-dedicated environment.

Ideal candidates bring 3+ years in clinical project management, lifecycle insight, and ability to drive study progress in fast-paced settings while maintaining regulatory compliance and effective stakeholder

Qualifications

• 3+ years of clinical project management experience.
• Experience running clinical trials from start-up through closeout.
• Experience supporting complex Phase 2b studies within inflammation.
• Strong CRO/vendor management and oversight experience.

Responsibilities

• Drive operational execution of a complex Phase 2b inflammation study from start-up through database lock and closeout.
• Independently manage day-to-day study operations with minimal oversight.
• Own timelines, deliverables, risks, and issue resolution across multiple workstreams.
• Partner cross-functionally to proactively identify risks and implement operational solutions quickly.
• Lead vendor management activities and maintain strong oversight of external partners and CROs.

Skills

Clinical project management

Phase 2b study experience

Vendor management

Cross-functional leadership

Tools

MS Word

MS Excel

PowerPoint

Job description

Syneos Health is seeking an Experienced Clinical Project Manager for inflammation studies. This remote-US role requires ownership of end-to-end trial execution, strong leadership of cross-functional teams, and hands-on oversight of vendors and CROs in a sponsor-dedicated environment.

Ideal candidates bring 3+ years in clinical project management, lifecycle insight, and ability to drive study progress in fast-paced settings while maintaining regulatory compliance and effective stakeholder