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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 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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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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An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stak...
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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A global pharmaceutical company, based in Uxbridge, is currently looking for a Senior Health Economics Manager to join their team. Working as part of a key team within the business you will further develop their impressive pipeline of future products...
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A global pharmaceutical company, based in Uxbridge is currently looking for a Senior Regulatory Affairs Manager to join their team. You will be a confident Regulatory Lead looking to work in an innovative therapy area, developing and defining regulat...
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...
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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Our client, a global pharmaceutical company, is currently looking for a CMC Regulatory Affairs Manager to join their team in Uxbridge on a temporary contract. This is a great opportunity to work for a pharmaceutical company who have created a centre ...
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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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...
Lab Technician required for market leading R&D organisation near Southampton: Responsibilities: Sample receipt, preparation, analysis, and reporting: Handling samples, preparing them for analysis, conducting analysis using appropriate methods, and re...
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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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Lab Technician required for market leading R&D organisation near Southampton: Responsibilities: Sample receipt, preparation, analysis, and reporting: Handling samples, preparing them for analysis, conducting analysis using appropriate methods, and re...
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Quality Assurance Officer- Batch Release - Global Pharmaceutical Company Contract: 12-Month Contract Location: Marlow, UK Salary: 32,000 p/a Working Pattern: Hybrid SRG are working with a Global Consumer Pharmaceutical company to help them find a Qua...
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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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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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Title - Quality Assurance Associate Location: Speke, Liverpool Rate: Circa 19.18 p/h Shift - M-F, 37.5 hrs Contract - 6 months SRG is working on an excellent opportunity for a Quality Assurance Associate to join a global-leading pharmaceutical manufa...
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