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Clinical Recruitment

2020 was our Clinical Team’s busiest year, for obvious reasons.

Our consultants work with both start-ups and established global businesses to ensure their talent pools are full of experienced candidates ensuring no delay to the clinical development, or testing phases of their products lifecycle.

Be it working with some of the world’s largest CROs and Bio-Pharmaceutical companies helping them to staff international clinical trials across Phases I to IV, or working with the clinical teams within the Pharmaceutical sector to ensure all clinically developed drugs make it to market – our team have the network of clients to provide you with opportunities for your next permanent or freelance position.

Clinical Trials

Whether phase I or phase IV of a clinical trial, at early planning stage or putting together a PMS team as products enters the market.

Either way our experienced consultants use their networks built up over an extended period within the industry to deliver opportunities (permanent & freelancers) on some of the most scientifically advanced Clinical trials operating in the world.

If you want to accelerate your experiences, then reach out to the team to discuss where we have clients in need.

Clinical Evaluation

- Can you put a CER together to order?
- Comfortable working on more than one at a time?
- Does the research element of the position of the role excite you?
- Does your current role allow you to do all of this from your home office?
- How CER’s are produced and where the work is done has been changing and that change has been accelerated this year.

Speak to a member of our team to hear what our clients are doing in this field today!

PMS and Post-market
Clinical Follow-up

Maybe it is the Post-market Surveillance team that you have built your career within?

You enjoy analysing how a product has impacted the market, and finding where changes can be made for future iterations of the product.

Our teams work with some of the most innovative companies within healthcare, so if it's the release of a new drug or a robotic arm we will have clients with products to excite you in your world of PMS

CRO

Frustrated at working on the same product day after day, year after year?

Clinical Research Organisations (CRO's) can offer you that variety.

Many young start-ups have very innovative exciting young ideas, they often need to outsource the research element of the product lifecycle to a CRO to ensure no delays are met.

Working for a CRO can give you access to some of the most forward-thinking products on the market, it gives you a variety of product and people you might not have ordinarily.

Reach out to the team for an informal discussion about the CRO world.

Read Our Blogs

Navigating IVDR Regulation (EU) 2017/746: What Medical Device and IVD Companies Need to Know

By Adaptive Life Science The European Union’s In Vitro Diagnostic Medical Devices Regulation (IVDR) — Regulation (EU) 2017/746 — represents one of the most significant regulatory overhauls in the diagnostics sector in decades. Officially applicable since 26 May 2022, the IVDR replaces the previous Directive 98/79/EC, introducing a more robust, transparent, and risk-based framework for […]

Cultural Fit Matters in Medical Devices

Why Cultural Fit Matters in the Medical Device Industry: Beyond Experience and QualificationsThe medical device industry operates at the intersection of precision, innovation, and compliance. Given the critical nature of its work, designing and manufacturing devices that directly impact patient care, it’s no surprise that experience and qualifications are often the top priorities when hiring. […]

ISO 13485:2016 Internal Audit Checklist – What Quality Professionals Need to Know

Published by Adaptive Life ScienceSpecialists in Medical Device, IVD, and Biotech Recruitment Why Internal Audits Matter in ISO 13485:2016 Internal audits are a cornerstone of any compliant Quality Management System (QMS) under ISO 13485:2016. For Quality Engineers, Regulatory Affairs professionals, and QMS leaders, these audits are not just about ticking boxes—they’re about ensuring product safety, regulatory readiness, […]

Are ISO Standards Mandatory for MDR Compliance?

In the medical device industry, compliance with regulations is crucial to ensure the safety and efficacy of products. For companies operating in Germany and across Europe, understanding the relationship between ISO standards and the Medical Device Regulation (MDR) is essential. Understanding MDR Compliance The European Union Medical Device Regulation (EU MDR 2017/745) sets out the […]

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