We specialize in placing highly educated and experienced Scientific, Research and Medical professionals who are at the forefront of groundbreaking new drug discovery, toxicology and pharmacology and who have the clinical trial design experience to bring new, safe and effective drugs to market. We have the network to provide candidates at Research Scientist level, all the way through to Chief Medical Officer and everything in between.

We’re able to source the very best Medical Monitors, Medical Writers, Medical Advisors/Directors and Medical Science Liaisons, as well as all levels of specialists within Drug Safety and Pharmacovigilance.

Our clients can rely on us to help them identify, hire and retain the best clinical professionals needed to ensure a smooth and complete clinical trial life cycle. This includes CTA’s and experienced CRA Monitors, to Trial Managers, Project Managers as well as Line Managers as senior as Global/Heads of Operations.

Looking for top talent within Biometrics? Then look no further. We have an extensive network and a proven track record of placing experienced Biostatisticians, Statistical & Clinical Programmers as well as Data Managers into Pharma, Biotech, CRO and Medical Device organizations. We provide quality candidates from entry level all the way through to VP, across a variety of therapeutic areas depending on your specific requirements.

We support our Pharmaceutical, Biotech and CRO clients across a wide range of skillsets and indications within the Regulatory space which includes Strategy, Operations, CMC, Labelling, OTC and Submissions.

We're also well-versed in sourcing and providing exceptional talent within Quality Assurance and Quality Compliance to ensure your business is providing safe and effective products which meet all the relevant regulatory requirements.

We have a separate team focusing purely on anything and everything Medical Device & Diagnostics focused. Our proficiency covers early phase Research and Development, Design, Engineering (Software, Mechanical, Electrical) through Clinical Trials to 510k Regulatory approval, Quality Assurance, Manufacturing and Post-Market.