Build the Clinical Teams That Get Therapies to Patients
Every day a clinical programme is delayed costs more than time.
EPM Scientific places the clinical development, clinical operations, biometrics, and pharmacovigilance professionals who keep trials on track and pipelines moving for pharma, biotech, and CROs.
Clinical talent solutions, bespoke to you
The right clinical hire at the right time makes all the difference. Here's how we help.
Hiring for your business
Clinical hiring demands a partner who understands the science, the regulations, and the timelines.
Looking for a new role?
Browse the latest clinical roles across pharma, biotech, and CROs, with expert support from first conversation to final offer.
Adding value
Compensation benchmarking, talent mapping, and market intelligence to help you hire smarter and move forward with confidence.
Specialist clinical expertise
Clinical professionals must combine rigorous scientific training with regulatory fluency and the operational discipline to execute in some of the most complex, high-pressure environments in life sciences. Finding that, and at the right seniority, therapeutic area, and geography, takes a specialist.
Clinical Development
Clinical development professionals define and drive the scientific strategy that takes a compound from first-in-human to regulatory submission. From protocol design to investigator relationships and agency interactions, these are the people who shape whether a programme succeeds. Deep therapeutic expertise and regulatory knowledge are non-negotiable. We support hiring across Clinical Research Physicians, Medical Monitors, Clinical Development Managers, Clinical Programme Leads, VPs of Clinical Development, Chief Medical Officers, and Therapeutic Area Leads.
Clinical Operations
Executing a clinical trial across multiple sites, countries, and regulatory environments demands exceptional operational talent. We find the clinical operations professionals who manage the people, processes, and systems that keep studies on time, on budget, and inspection-ready. We place specialists across Clinical Research Associates, Clinical Trial Managers, Study Start-Up Managers, Site Activation Leads, Heads of Clinical Operations, VPs of Clinical Operations, and Directors of Project Management.
Biometrics
Behind every regulatory submission is a robust biometrics function. Biostatisticians, statistical programmers, and data managers ensure that clinical data is collected, analysed, and presented with the rigour that regulators demand. In an era of adaptive trial designs and AI-driven analytics, this function has never been more strategically critical. Our expertise spans Biostatisticians, Senior Biostatisticians, Statistical Programmers, SAS Programmers, Data Managers, Clinical Data Scientists, Heads of Biometrics, and VPs of Biostatistics.
Pharmacovigilance
Pharmacovigilance professionals monitor, assess, and report on the safety profile of products throughout their lifecycle, ensuring compliance with evolving FDA, EMA, and global regulatory requirements. With increasing scrutiny on post-market surveillance, this is an area that organisations cannot afford to understaff. Roles include: PV Associate · Safety Scientist · Medical Safety Officer · Pharmacovigilance Manager · Signal Detection Specialist · QPPV · Head of Pharmacovigilance · VP of Drug Safety
TESTIMONIALS
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