Services
The right clinical people, in the right countries.
From a single CRA covering three sites to several roles across Europe, we supply experienced professionals on contract, working under your direction and to your SOPs. And when you want someone in your own team for the long term, we recruit permanent hires too.
Who we work with
Sponsors of every size, across drugs, biologics and devices.
Biotech
From first-in-human studies to pivotal trials: experienced people on the ground without building a European team of your own.
Pharmaceutical
Small and large pharma: extra capacity for a single study, specialist skills, or cover across a portfolio, contracted for the time you need.
Medical devices
CRAs and project managers for clinical investigations under the UK and EU medical device regulations, sized to your sites.
Individual placements
One role, filled well.
Need a CRA for your London and Manchester sites, or a regulatory specialist for an MHRA submission? We send you a short, vetted shortlist and handle everything after you choose.
- Freelance contractors, engaged through their own company, as self-employed professionals in their own country, or through an umbrella company
- Engaged on contracts that match your contract with us
- Hourly, a fraction of an FTE, a set number of days a month, or full time
- Contract lengths from a few weeks to the life of the study
Multi-role recruitment
Several roles, recruited together.
For sponsors who need people in several roles or countries. You tell us the roles and time commitment. We recruit and contract each person, and you direct their work.
- Roles and time commitments agreed with you
- Project managers, CRAs, regulatory and site support professionals
- Add or reduce contracted time when you ask
- One contract and one monthly invoice for the whole team
Permanent hires
The right person, for the long term.
When a role belongs in your own team, we find and vet candidates in the same way as our contractors. You interview, choose and employ them directly.
- CRAs, project managers, regulatory and start-up specialists across the UK and Europe
- The same checks as every contractor: experience, GCP training and right to work, with two references spoken to by phone
- A shortlist from people who know clinical operations, not just keywords on a CV
- Contract to permanent: start someone on contract and take them on permanently later, for a fee agreed at the outset
Roles we recruit
Clinical operations, end to end.
Medical device studies
People who know clinical investigations.
Device studies run differently from drug trials. We place professionals who have worked on clinical investigations under the UK and EU medical device regulations.
- CRAs experienced in device studies, from early feasibility to pivotal and post-market follow-up
- Device regulatory specialists for MHRA and EU competent authority submissions
- Clinical evaluation, vigilance and post-market follow-up support
Compare
Which option fits?
| Feature | Individual placement | Multi-role recruitment | Permanent hire |
|---|---|---|---|
| Best for | Specific roles for a defined period | Several roles or countries at once | A long-term role in your own team |
| How they are engaged | Contract, via their own company, self-employment or an umbrella company | Contract, via their own company, self-employment or an umbrella company | Employed directly by you |
| Time commitment | Hourly to full time | Each role sized separately, from hourly to full time | Full or part time, as you employ them |
| Who directs the work | You | You | You |
| Overseas entity needed | No | No | Yes, or an employer of record in that country |
| How you pay | Monthly, for hours or days worked | One consolidated monthly invoice | A one-off fee when they start |
Tell us what your study needs.
Enter your countries and sites in the team planner to see a suggested mix of people and an indicative monthly cost.