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Staff augmentation for drug safety, clinical operations and clinical development.
Flexible, compliant staffing for sponsors and CROs, from a single specialist to a full project team.
The roles we fill
Drug Safety and Pharmacovigilance
Support for safety operations from case intake to aggregate reporting.
- Case processors and safety associates
- Safety scientists
- Aggregate report writers
- PV quality and compliance specialists
Clinical Operations
Hands-on trial execution talent to start studies faster and keep them moving.
- Clinical research associates
- Clinical trial managers
- Study start-up and site management
- Clinical trial associates
Clinical Development
Scientific and strategic expertise to design, run and report on clinical programs.
- Clinical scientists
- Clinical program leads
- Medical monitoring support
- Protocol and study document specialists
Contract staff augmentation
Add specialists to your team for a defined project or longer term, without adding permanent headcount.
Contract-to-hire
Work with a professional first, then convert to a permanent role when the fit is proven.
Direct hire
We find and present candidates for permanent roles, and you hire directly.
Every candidate is screened before submission
Depending on the role and your requirements, this includes:
Experience, education and license or credential verification
Exclusion and debarment list checks
Background and reference checks as required by the client
Confidentiality and data privacy safeguards
Need a specialist on your team?
Share the role, timeline and engagement length, and we will confirm scope within a business day.
