Clinical Project Specialist - Contract Position
ProTrials
WorldwideFully remoteContractMid LevelHealthcare & Telemedicine
Posted 5 hours ago5h agoApply link checked 5 hours ago
Why we think you can apply
- Hiring model
- Open worldwide · the employer states no country restriction
- Work from
- Anywhere, the UAE included
Posted 5 hours ago · apply link checked 5 hours ago
About the role
Responsibilities
- Partner with project leadership, sponsors, sites, and cross-functional study teams from start-up through close-out
- Support study planning and site activation
- Ensure TMF quality and inspection readiness
- Manage vendors and track critical project deliverables
- Mentor CTA team members and collaborate directly with sponsors
Requirements
- Proactive and highly organized clinical research professional
- Experience in hands-on study coordination and project oversight
- Ability to manage complex studies and anticipate project needs
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, supporting innovative treatments in the pharmaceutical, biotech, and medical device industries.
What we look for
- Clinical research experience
- Study coordination skills
- TMF quality management
- Vendor management experience
- Project oversight capabilities
Project ManagementClinical ResearchTMF
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ProTrials
SponsorWake up to a shortlist, not a search results page.
NeverApply scores every new listing against your CV, salary floor and visa. A handful of real matches by morning.
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