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About the role

GForce Life Sciences is seeking a results-oriented Clinical Project Manager to oversee multi-site trials and ensure on-time, within-budget delivery. You will coordinate cross-functional teams, manage timelines, and supervise regulatory submissions with oversight from Regulatory Affairs. Responsibilities include protocol input, budget tracking, vendor management, and maintaining study quality. The role is 4 days onsite across Plano, Maple Grove, Santa Clara, Sylmar, CA and other sites, with a

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JOB OVERVIEW

Experience level

Mid

Location

Plano, TX

Occupation

Project Management Specialists

Industry

Research and Development in Biotechnology

Posted

today

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