Clinical Project Specialist - Contract Position

Responsibilities

• Partner with project leadership, sponsors, sites, and cross-functional study teams from start-up through close-out
• Support study planning, site activation, TMF quality and inspection readiness, vendor management, and the tracking of critical project deliverables
• Take ownership of important study activities
• Mentor CTA team members
• Collaborate directly with sponsors
• Contribute to the quality and operational success of clinical trials

Requirements

• Proactive, highly organized clinical research professional
• Experience in clinical trial execution and project oversight
• Experience in site activation and TMF quality management
• Experience in vendor management and tracking project deliverables

About the Company

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Founded with a clear mission to deliver high-quality, experienced, and ethical services, we've supported research behind innovative treatments in the pharmaceutical, biotech, and medical device industries. We believe great work happens when team members feel valued, supported, and empowered. At ProTrials, you'll join a collaborative community committed to making a meaningful impact on global health.