Our Services

Recruitment Services for Clinical Research

Contingency-based direct hire placement. You only pay when someone starts.

Direct Hire Placement

Our core service: we find, vet, and present clinical research professionals who match your site's operational needs.

1

Intake & Calibration

We learn your site's therapeutic focus, phase requirements, EDC systems, team culture, and specific operational needs. This calibrates our AI screening rubric to your site.

2

Sourcing & AI Screening

Our proprietary AI evaluates candidates across 4 dimensions: technical/regulatory knowledge, operational/systems proficiency, soft skills, and logistical fit. Each candidate receives a competency score (0-100).

3

Human Review & Vetting Memo

Our clinical research consultants personally review every AI-screened candidate. Those who pass receive a 3-sentence Vetting Memo explaining their operational fit for your specific role.

4

Shortlist Delivery

You receive a curated shortlist with Vetting Memos — not a stack of resumes. Expect your first shortlist within 5-7 business days of intake.

5

Interview & Offer Support

We coordinate interviews, provide candidate prep, and assist with offer negotiation to ensure a smooth hiring process.

The Vetting Memo

We never present a candidate without a Vetting Memo. This 3-sentence consultant note is written by our team after reviewing the AI screening results and the candidate's full profile.

Each memo addresses: operational fit (can they do the day-to-day work?), system proficiency (are they fluent in your EDC/CTMS?), and cultural/regulatory alignment (will they thrive at your site?).

Example Vetting Memo

“Maria brings 8 years of oncology CRC experience across Phase II-III trials with strong SAE reporting and ALCOA-C documentation practices that align directly with Meridian's operational requirements.”

“Her Medidata Rave proficiency is advanced — she has built edit checks and managed query resolution across multi-site studies, which is critical for Meridian's current 12-site oncology program.”

“Her leadership in training junior CRCs and managing sub-investigator documentation makes her a natural fit for the Senior CRC role, where she would be expected to mentor the team while maintaining her own patient caseload.”

Transparent Fee Structure

Standard
20%
of first-year base salary
  • Contingency-based: pay only when someone starts
  • 90-Day Success Guarantee included
  • 12-month candidate ownership
  • Net 30 payment terms
Enterprise
18%
of first-year base salary
  • Available for 3+ placements within 6 months
  • All standard benefits included
  • Priority sourcing and dedicated account manager
  • 5% consulting credit toward a Site Operations Audit

Roles We Specialize In

Clinical Research Coordinator (CRC)
Senior / Lead CRC
Clinical Research Associate (CRA)
Clinical Trial Manager (CTM)
Clinical Data Manager
Regulatory Affairs Coordinator
Regulatory Affairs Specialist
Site Director
Quality Assurance Auditor
CTMS Administrator
TMF/eTMF Specialist
Principal Investigator Support

Discuss Your Staffing Needs

No obligation. Tell us about your open roles and we will explain how we can help.