Clinical development runs on people who can hold a protocol, a site and a timeline in their head at the same time. Sponsors and research teams come to us when they need monitors who can close a backlog of visits, trial managers who can recover a slipping study, or data professionals who can get a database to lock on schedule. If that describes your work, we want to hear from you.
What hiring teams look for
Most clinical roles we fill ask for hands-on experience under ICH GCP, familiarity with the phase and therapeutic area of the study, and confidence with the systems the sponsor already uses, such as an EDC platform, a CTMS or an eTMF. Hiring managers value candidates who can describe specific outcomes: sites they activated, queries they resolved, audits they prepared for. Certifications help, but a clear account of what you personally owned on a study helps more.
We recruit at every level, from early-career clinical research associates building their first monitoring experience to senior trial leaders who have run global programs. Roles may be onsite, hybrid, regional with travel, or fully remote, depending on the study and the sponsor.
Engagement types
Many clinical roles are contract assignments tied to a study phase, often with the option to extend or convert. Others are direct-hire positions with sponsors building permanent teams. Your recruiter will explain the expected duration, the travel commitment and the realistic chance of extension before you decide to apply.
Therapeutic areas
Our recruiters regularly place professionals with experience in cardiovascular, metabolic, neurology, nephrology, psychiatry, infectious diseases, hematology and oncology studies.
Roles we recruit for
- Clinical Research Associate (CRA)
- Senior and lead CRA
- Clinical Trial Manager
- Clinical Project Manager
- Clinical Trial Assistant
- Clinical Data Manager
- Clinical Data Coordinator
- Biostatistician
- Statistical Programmer (SAS)
- Drug Safety Associate
- Pharmacovigilance Scientist
- Medical Writer
- Clinical Quality Assurance Auditor
- Study Start-up Specialist
- SAS Programmer
- Clinical Scientist
How we help you
A recruiter who knows clinical operations reviews your profile, talks through the studies you have supported and matches you to roles that fit your experience and travel preferences. We submit you only with your consent, prepare you for the client's interview format and tell you how it went. If a role is not right, we say so and keep looking.