As clinical professionals, you work with precision – and so do we
At SRG, we’re a leading recruiter of clinical jobs in the UK and Europe. In the current market, many companies are finding it difficult getting hold of the right talent. So if you’re a specialist or a senior management-level scientist looking to nurture your niche, our network gives us access to fantastic contract and permanent roles with many of the world’s top pharmaceutical, biotechnology and clinical research organisations.
We cover all areas of clinical research, including:
- Clinical operations
- SAS programming
- Data management
- Medical information
- Medical affairs
- Regulatory affairs
Take a look at our clinical jobs below and contact us if you’d like further information.
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The Role:Responsible for highlighting potential delaying factors promptly to line management and sharing knowledge of regulatory documentation and procedures with others to assist in problem...
Freelance (Contract) Study Start-Up Specialist (Medical Devices)Contact duration: min 12 monthsLocation: office-based in OxfordshireFreelance Study Start-Up Specialist (Medical Devices) highly advanced and exciting opportunity is...
Partnering with Non-Clinical Development in facilitating the quality mind-set into the preclinical portfolio across our clients sites. This position will support operations related to...
Senior Statistician Innovative BiopharmaClinical Perm Full-TimeUp to £50K pr. annum + BenefitsCambridgeshire I am looking for an experienced Clinical Trial Statistician for Biopharmaceutical Company who...
The Role: Provide comprehensive support to the Regulatory Affairs and Clinical Operations teams to coordinate the logistical and regulatory aspects of the clinical trials in...
Freelance (Contract) Clinical Research Associate (Medical Devices)Contact duration: min 12 monthsLocation: office-based in OxfordshireFreelance CRA/Clinical Research Associate (Medical Devices) highly advanced and exciting opportunity is...
The Role:Responsible for preparation of high quality, Chemistry, Manufacturing and Control detailed regulatory documents using varied information sources. Working to agreed deadlines and maintaining records...
Are you an accredited QP?Then this could be a great opportunity for you to join a reputable organisation based in Salisbury as a QP!As a...
The role:Performance of pre and post approval regulatory activities to ensure compliance with the Falsified Medicines Directive. Key Responsibilities:Preparation and submission of MA variations, Article...
Senior Medical Writer Permanent role office-based Cheshire, UKPermanent opportunity Competitive salary Excellent benefit package Coaching and Training Great opportunity to join a growing global Medical...
>View all Clinical jobs