We place credentialed professionals who know the systems, standards, and pace of real-world research and diagnostics.
Staffing Roles
Don’t see the exact role you need? Reach out and let us know.
Supports study teams in meeting recruitment goals while ensuring protocol and ethical compliance.
Manages study teams, vendors, and sites to drive operational excellence.
Works closely with cross-functional teams to facilitate approvals and maintain ongoing regulatory compliance.
Oversees daily trial activities at the site level, ensuring compliance with protocols, GCP, and regulations.
Ensures trials meet regulatory, SOP, and GCP standards while overseeing quality processes.
Ensures data accuracy, consistency, and compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP).
Serves as the primary point of contact between sponsors, CROs, and study sites.
Supports investigators, coordinates with study teams, and ensures the integrity and accuracy of clinical trial data.
Don’t see the exact role you need? Reach out and let us know.
Why Us
Get qualified staff on-site in 24–72 hours.
All professionals are background-checked and compliance-ready.
Real people available day, night, and weekends.
Coast to coast, we’re placing professionals every day.
How It Works
We’ve streamlined the life science staffing process so you can get qualified support when and where you need it most.
1
Tell us what you need, role, shift, location, and we’ll get to work right away.
2
We hand-select professionals from our vetted pool based on experience, credentials, and fit.
3
Log in anytime to track confirmations, review schedules, and approve timesheets with ease.
4
We manage staffing, vetting, and scheduling so your team can concentrate on the work that matters.
As a client, you’ll get access to our intuitive staffing platform that is built to save you time and streamline your workflow.
Easily request staff, approve timesheets, view schedules, and track fill rates in real time.
Real Results
From clinical trials to regulatory compliance, we deliver professionals who support breakthrough discoveries and bring life-changing therapies to market.
We provide experienced clinical operations professionals including CRAs, Project Managers, and Research Nurses to support every phase of drug and device trials in pharmaceutical, biotech, and academic settings.
Our experts in regulatory affairs, quality assurance, and GxP compliance ensure products meet FDA and international standards throughout development and post-market stages.
We staff Pharmacovigilance Associate Directors, Managers, Drug Safety Specialists and Adverse Event Reporting Coordinators ensuring accurate reporting, and support global pharmacovigilance efforts.
We support Medical Affairs teams with professionals like Medical Science Liaisons and Clinical Specialists who help translate research into practice, supporting education, engagement, and data communication throughout the product lifecycle.
FAQ
Quick answers to questions you might have about life science staffing.
We typically staff roles within 24–72 hours, depending on credentialing needs and job type. Fast turnaround is built into our process.
We’re headquartered in New York City, with regional offices in New York, Connecticut, California, and Florida.
Every candidate is license or certification-verified, competency-tested, and background-checked before placement.
Absolutely. We support repeat placements and long-term assignments where continuity matters most.
TemPositions Health Care manages payroll, benefits, workers’ comp, and compliance so you can focus on your projects.
Contact Us
We’ll follow up within 24 hours with next steps, qualified candidates, or whatever you need to keep your research and operations moving forward.
From front-end access to backend analytics, we deliver revenue cycle professionals who keep operations efficient and profitable.