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This role will be to join the UKHSA SIREN study team. SIREN (SARS-CoV-2 Immunity & Reinfection EvaluatioN) is a large-scale study of health care workers, focused on increasing our understanding of whether individuals with COVID-19 are protected from ...
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Clinical Data Manager | 12-month FTC | Cambridgeshire (work from home options) A unique opportunity for an accomplished Clinical Data Manager to join a leading laboratory changing clinical practice Our client is a key player within medical devices se...
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Clinical Trials Manager Virology, management of central lab EMEA The CTM role will involve regional management on Phase Ib-III clinical studies, with a strong emphasis on the EMEA region. The successful candidate will be a member of the Global Study ...
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FTC until end of Dec 2024 (3 days a week) Salary Negotiable dependent on experience plus benefits Scope My client are an expanding pharmaceutical manufacturing organisation seeking a highly motivated and experienced Quality Assurance Manager to join ...
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Please note this is opportunity is a 12 month FTC. Our client is a leading medical equipment manufacturer, they are seeking a skilled Project Management professional to join their PMO team and lead the delivery of various commercial programs across t...
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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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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...
Global Regulatory Affairs - Due Diligence Manager / Senior Manager Your new company This US Biotech are looking for a Regulatory Affairs professional with strong Due Diligence experience to join an exciting, high-profile project, this is initially a ...
Regulatory Affairs Manager - UK and Ire Cosmetics Your new company This household name is looking for an experienced Regulatory Affairs Manager / Senior Manager to join their UK and Ire Cosmetics team. This role is mostly remote with 2 days required ...
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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My client, a leading a research agency in London is hiring for the two positions and will consider candidates at Senior Research Executive and Research Manager level. One position will sit within the Community team (welfare, housing etc) and the othe...
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Contract until end of Dec 2024 (3 days a week) Salary Negotiable dependent on experience plus benefits Scope My client are an expanding pharmaceutical manufacturing organisation seeking a highly motivated and experienced Quality Assurance Manager to ...
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Regulatory Affairs CMC Manager - International markets Your new company This well-known biotech is looking for an experienced Regulatory Affairs CMC Manager to join their well-established team on a contract basis. This role will mostly be managed fro...
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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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Regulatory Affairs Labelling Associate Project Manager contract job Your new company This well-known biopharmaceutical company is looking for a Regulatory Affairs Labelling Associate Project Manager to join their Labelling team on a contracting basis...
The Senior Technologist positions are integral to the successful execution of scientific activities outlined in project Science Plans. With a focus on ensuring alignment with the organisation's R&D portfolio and broader business objectives, this role...
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Long Term Work at Household Name. On site Parking, Great Team , Lovely working environment 14.25 per hour. As a Laboratory Technician, you will have a specific focus on supporting the Laboratory Supervisor in the following: Responsible for the mainte...
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Work at Household Name. Onsite Parking, Great Team , Lovely working environment 14.25 per hour. As a Laboratory Technician ??????? , you will have a specific focus on supporting the Laboratory Supervisor in the following: Responsible for the maintena...
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Batch Release Co-ordinator - 18.00 Based on Site in Liverpool. 12 Month Contract The role holder is responsible for working cross-functionally and reviewing and compiling batch specific documentation and data for batch release, ensuring compliance wi...
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Synthetic Organic Chemist I am currently recruiting a Synthetic Organic Chemist on behalf of one of our clients, a chemical company. Role overview: Hiring manager is looking for a highly motivated Chemist, eager to kick- start or further grow their c...
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QC Technician Our client is a well-established organization based in the Birkenhead/Merseyside area, and actively seeking to recruit an experienced QC Technician to join their Quality department on a three-month contract. Ideally, the candidate would...
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Technical Web Analyst Teleco London - 3 days per week in the office 500- 570 per day (inside IR35) Join a dynamic team at the forefront of digital transformation within the telecoms industry. Our client is a leading telecommunications company committ...
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Digital Implementation Specialist Teleco London - 3 days per week in the office 500- 570 per day (inside IR35) Join a dynamic team at the forefront of digital transformation within the telecoms industry. Our client is a leading telecommunications com...
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Job title: Senior Analyst Location: Abingdon, Oxfordshire (on site full time) Contract length: Until 31/04/2025, covering maternity leave Pay rate: 35,000 per annum My client is part of a family of businesses, bringing together exceptional teams of e...
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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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