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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...
Manufacturing Technician
OXFORDSHIRE, GB
...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...
Clinical Research Associate
£40000 - £60000/annum
OX11, DIDCOT, OXFORDSHIRE, OX11
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...
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Manufacturing Technician
WITNEY, SOUTH EAST ENGLAND
...Produce prototypes, pre-clinical, and clinical trial products in a cleanroom facility /li li Conduct performance and product testing /li li Maintain and calibrate equipment, ensuring cleanliness of the facility /li li Contribute to process optimisation, risk management, and waste reduction /li...
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...
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Manufacturing Technician
OXFORDSHIRE, SOUTH EAST ENGLAND
...of prototypes, pre-clinical and clinical trial products for projects in ISO 8 cleanroom facility. Manufacturing batches to time and GMP standards. /li li Cleaning and calibration of facilities equipment /li li Cleaning and helping with monitoring of clean room facility /li li Updating...
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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 Manager
MAIDENHEAD, GB
...deliverables for global clinical trial applications in accordance with the overarching global regulatory strategy considering regional specific requirements Coordinate submission strategies for global clinical trials, ensuring alignment with regulatory strategies, and promptly highlighting any...
Manager, Clinical Trial Strategy & Submissions, Regulatory Operations
MAIDENHEAD, GB
...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 Trial Specialist
MAIDENHEAD, GB
...affairs within clinical trials. Responsibilities: Oversee a portfolio of CTAs, managing the preparation and dissemination of documentation for new initial CTAs and all CTA maintenance activities, including substantial amendments and end-of-trial notifications. Offer guidance on...
Regulatory Affairs Consultant
SLOUGH, ENGLAND, UNITED KINGDOM
...related aspects of clinical trials. You will serve as the main point of contact and be responsible for delivering submission-specific milestones while offering guidance on submission strategies. Additionally, you will actively participate in EU-CTR consulting and contribute to the operational...
Regulatory Specialist
MAIDENHEAD, GB
...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...
Senior/Principal HTA Statistician
WOKINGHAM, GB
...medicine by analysing clinical trial data, providing statistical consultancy, and mentoring junior colleagues. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities Apply innovative statistical approaches to solve novel data...
Regulatory Affairs Coordinator
MARLOW, 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...
Real World Data Manager
SLOUGH, GB
...as a data manager with Clinical trial / Real World Data experience is essential Strong proficiency with EDC platforms for clinical data collection. Deep understanding of data management processes and standards. Experience attending client calls and being comfortable being client facing Experience...
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...
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...
Regulatory Manager, Clinical Trial Strategy & Submissions
£65 - £75/hour
MAIDENHEAD, BERKSHIRE, SL6
...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...
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