Location: Hybrid in Fairfield County, Connecticut
Help accelerate cures. Change the future of oncology.
My client—one of the most influential forces in cancer research—is expanding its clinical operations team. If you’re driven by purpose and thrive in fast-moving, mission-anchored environments, this is your opportunity to contribute directly to life-extending therapies.
Why You Should Apply
- Work on cutting-edge adaptive platform trials impacting real patient outcomes
- Hybrid flexibility + collaborative, mission-centric culture
- Competitive compensation + full benefits package
- Join an organization that has helped deliver 15+ FDA-approved therapies
- Make a measurable impact in oncology research every single day
What You’ll Be Doing
- Support operations for complex oncology trials, including site, vendor, and CRO communication
- Maintain IRB submissions, trial documentation, and study systems
- Track clinical data, drive timely data entry, and manage safety reporting workflows
- Coordinate with drug depots, ensure inventory continuity, and partner with cross-functional teams
- Build presentations, reports, and operational tools that keep trials running smoothly
About You
- 5+ years oncology clinical trial coordination/management
- Strong communicator & problem-solver with impeccable attention to detail
- Skilled with MS Office, study systems, and GCP/ICH guidelines
- Collaborative, flexible, and motivated by purpose
How To Apply
Email
Emily@scientificsearch.com with Job #19678 in the subject line.