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Regulatory Specialist (CMC) Clinical Development
Our client is a global leader in the pharmaceutical industry, committed to advancing science and delivering innovative therapies to patients worldwide. To support ongoing clinical development activities, we are...
Hybrid CMC Regulatory Specialist - Clinical Submissions
Actalent is seeking a Regulatory Specialist (CMC) to drive global regulatory submissions for clinical-stage products and to support IMPDs, CTAs and related CMC documentation. You will liaise with cross-functional...
Clinical Site Safety & Environment Lead
Actalent in Switzerland is seeking a Clinical Site SHE Coordinator to develop and implement an overarching safety, health and environmental strategy for the clinical supply chain. The role includes coordinating...
Clinical Site SHE Coordinator
If you have experience in Safety, Health, and Environmental activities within clinical supply chain, this role might be perfect for you! We are looking for a Clinical Site SHE Coordinator to develop and implement an...
Global Medical Device Project Manager - Engineering Lead
Actalent is seeking a Device Engineering Project Manager in Dublin to lead development and improvement of medical devices. You will coordinate cross-functional teams across engineering, clinical, regulatory and...
Medical Device Project Manager
I'm working with a global leading pharmaceutical company that’s currently seeking a Device Engineering Project Manager based in Dublin . This role involves leading the development and improvement of medical devices,...
Clinical Research Nurse
Clinical Research Nurse – 6-Month Contract Location: Bromley Contract Type: 6-month contract Hours: Full-time About the Role We are looking for a Clinical Research Nurse to join one of our clients, a leading global...
Onsite Clinical Research Coordinator – London
Actalent is seeking a Clinical Research Coordinator in London, UK, for an onsite role with opportunities to start immediately. The candidate should have a minimum of 2 years of clinical research experience and be...
Clinical Data Specialist — Oncology Research
A leading staffing and consulting firm is seeking a Clinical Data Manager in Taunton. The ideal candidate will have at least one year of clinical research experience and be capable of working independently or as part...
Clinical Trial Coordinator
Contract length: Short term contract with possibility of extension About the Role An exciting opportunity has become available for a Clinical Research Coordinator to support the delivery of innovative clinical...