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Hybrid working 2x a week Scope: This is an excellent opportunity for an experienced Clinical Trial Submissions Manager to join a global pharmaceutical company for an initial 12 months with the potential for this to be extended. This role has come abo...
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SRG are currently looking for a Regulatory Affairs Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead. The Role: Delive...
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Job Title: Regulatory Affairs CTA, CTR Manager/Consultant (Inside IR35) Job Type: 12-month contract Location: Berkshire, UK – Hybrid Pay Rate: 65-75 per hour (PAYE) We are partnered with a leading Pharmaceutical organization who are looking for an ex...
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Quality Assurance Manager - Good Clinical Practice Our client, based in Cheshire are recruiting for a contract GCP QA Manager to join them for a 6 month project. This is an exciting opportunity to join a dynamic company with a great culture. Role: Pr...
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Are you a Trial Master File expert looking for your next role? Then, Cencora Pharmalex is your career opportunity Cencora PharmaLex is looking for an experienced Senior Trial Master File Study Owner to work within our Professional Services team on a ...
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