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Clinical Trial Operations Specialist
BRACKNELL, ENGLAND, UNITED KINGDOM
CLINICAL TRIAL OPERATIONS SPECIALIST 12 Months Contract OUR COMPANY At Boehringer Ingelheim we develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company, we focus on long-term performance. We believe...
Clinical Trial Operations Specialist
BRACKNELL, SOUTH EAST ENGLAND
p b CLINICAL TRIAL OPERATIONS SPECIALIST /b /p p br /p p 12 Months Contract /p p br /p p b OUR COMPANY /b /p p At Boehringer Ingelheim we develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned...
Associate Director, Clinical Pharmacology
SURREY, ENGLAND, UNITED KINGDOM
...The Associate Director, Clinical Pharmacology is responsible for leading clinical research activities with focus on clinical pharmacology phase I pharmacokinetics and bioequivalence trials. He/she will ensure that high quality expertise is provided to meet state-of-the-art scientific, industry and...
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Associate Director, Regulatory Affairs CMC
£80 - 100
ABINGDON
...teams throughout clinical development and commercial lifecycle. br Key responsibilities will include authoring CMC modules/updates, including life cycle management; and generation of submission-ready content for the Quality/CMC sections of all clinical trial and marketing authorisation...
Sr Site Enablement Solutions Project Lead
READING, , UNITED KINGDOM
b Role Overview: /b br br The Site Enablement Solutions team at IQVIA provides qualified, clinically experienced research staff to clinical trial sites globally to accelerate and optimize the performance of clinical trials. By supplying sites with support for data entry, patient recruitment...
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Manager, Clinical Trial Strategy & Submissions, Regulatory Operations
MAIDENHEAD, ENGLAND, UNITED KINGDOM
...submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team and study teams. Ensure study deliverables are achieved in accordance with global regulatory...
Clinical Research Associate
OXFORDSHIRE, ENGLAND, UNITED KINGDOM
Cure Talent are delighted to be partnered with an established Medical Devices Manufacturer, who, due to their continued growth, have an exciting opportunity for an experienced Clinical Research to join them. As the new Clinical Research Associate, you will be responsible for overseeing trial sites...
Senior Clinical Project Manager
SURREY, ENGLAND, UNITED KINGDOM
Title: Senior Clinical Project Manager Salary: Highly Competitive Location: Surrey area (Hybrid) If you have a clinical background and are interested in joining an exciting international organisation then this could be the role for you! This company is a leading biotech with products on the market...
Program Manager (Clinical Trials/Managed Access)
WEYBRIDGE, ENGLAND, UNITED KINGDOM
...expertise within the Clinical Trial and/or Managed Access world to develop and maintain client relationships responsible for the delivery of new and existing patient access programs for key pharmaceutical and biotech accounts. Key Responsibilities: Lead the delivery of objectives for key...
Regulatory Specialist
MAIDENHEAD, ENGLAND, UNITED KINGDOM
...expertise for Clinical Trials. They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes. Key Responsibilities: Manage a portfolio of CTAs including preparation and distribution of documentation...
Regulatory Affairs Associate (EU)
SURREY, ENGLAND, UNITED KINGDOM
Regulatory Affairs Associate The Regulatory Affairs Associate will be responsible for: Managing the clinical trial applications in Europe and other selected countries Keeping up to date with regulatory and legal changes in EU Preparing pre- and post-authorisation regulatory documentation and...
Regulatory Affairs Coordinator
WINDSOR, ENGLAND, UNITED KINGDOM
...experience ideally in clinical trials and CTR submission experience would be preferred. Job Responsibilities include a portfolio of CTAs including preparation and distribution of documentation associated with new initial CTAs and all CTA maintenance activities such as substantial amendments...
Team Administrator / Coordinator Comparators
MARLOW, ENGLAND, UNITED KINGDOM
...owned pharmaceutical clinical trials supply organisation, with specialist divisions in Comparator Sourcing, Secondary Packaging & Labelling and Global Storage & Distribution. Our story is one of incredible growth and success, which has culminated in receiving many prestigious awards, such as...
Manufacturing Technician
WITNEY, ENGLAND, UNITED KINGDOM
...Produce prototypes, pre-clinical, and clinical trial products in a cleanroom facility Conduct performance and product testing Maintain and calibrate equipment, ensuring cleanliness of the facility Contribute to process optimisation, risk management, and waste reduction Experience Needed: Basic...
Senior Data Analyst - Biotechnology
OXFORDSHIRE, ENGLAND, UNITED KINGDOM
...scale biological and clinical datasets. Collaborate closely with interdisciplinary teams including researchers, bioinformaticians, and software engineers to design and execute data-driven experiments and analyses. Develop predictive models and algorithms to support drug discovery, biomarker...
Manufacturing Technician
OXFORDSHIRE, ENGLAND, UNITED KINGDOM
...of prototypes, pre-clinical and clinical trial products for projects in ISO 8 cleanroom facility. Manufacturing batches to time and GMP standards. Cleaning and calibration of facilities equipment Cleaning and helping with monitoring of clean room facility Updating quality records and...
Snr Clinical Trial Manager - Cell Therapy
LONDON (CITY OF LONDON), SOUTH EAST ENGLAND
p br Proclinical are seeking a dedicated Snr Clinical Trial/ Program Manager to accelerate the initiation and execution of Advanced Therapy Medicinal Products (ATMPs) clinical trials within one of our London based biotech clients. br Responsibilities: br - Streamline the clinical trial initiation...
Manager, Clinical Trial Strategy & Submissions, Regulatory Operations
MAIDENHEAD, SOUTH EAST ENGLAND
...submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team and study teams. /li li Ensure study deliverables are achieved in accordance with global...
Clinical Trial Assistant
LONDON, SOUTH EAST ENGLAND
ul li Role: Clinical Trial Assistant (CTA / Associate CPM) /li li Location: Hybrid (4 days remote and 1 day per week in London) /li li Company: Small Biopharmaceutical Company /li li Salary: £35,000 - £42,000 (depending one experience) /li /ul p br /p p RBW Consulting are...
Clinical Trial Manager
LONDON (UXBRIDGE), SOUTH EAST ENGLAND
p b Join the Virology Adventure! /b /p p br /p p Are you ready to embark on an exciting journey in the world of Virology? /p p We are seeking adventurous souls to join our team as a Clinical Trials Manager! /p p If you're passionate about making a difference in healthcare and thrive in...
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