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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 Specialist Apprentice
FARNBOROUGH, HAMPSHIRE, FARNBOROUGH, HAMPSHIRE
Description Clinical Trial Specialist Apprentice Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our...
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...
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Senior Legal Counsel - Supply & Technology Solutions (S&TS)
£100 - 125
SLOUGH
...amp; supply, clinical trial supplies, distribution, logistics & warehousing, IT related services, development & other services, licensing, construction projects and other agreements and issues specific to the biopharmaceutical sector. /li li Day to day support to global...
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...
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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...
Experienced Clinical Research Associate
45773
READING, BERKSHIRE, READING, BERKSHIRE
...i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability Administer protocol and related study training to assigned sites...
Senior Clinical Data Manager - FSP (oncology experience)
58481
MAIDENHEAD, BERKSHIRE, MAIDENHEAD, BERKSHIRE
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions...
Local Clinical Study Manager - UK
61634
MAIDENHEAD, BERKSHIRE, MAIDENHEAD, BERKSHIRE
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions...
Senior Clinical Data Manager - single sponsor
41408
MAIDENHEAD, BERKSHIRE, MAIDENHEAD, BERKSHIRE
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions...
TMF Manager
69043
READING, LONDON (GREATER), READING, LONDON (GREATER)
Job Purpose Responsible for efficient and appropriate management of Trial Master Files (TMF) and other TMF related, inspection relevant documents from creation through archival in compliance with applicable SOPs, processes and study specific requirements for assigned trials according to established...
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...
Study Start-Up Project Manager (Ethics and Regulatory Submissions)
63451
MAIDENHEAD, BERKSHIRE, MAIDENHEAD, BERKSHIRE
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions...
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...
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
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 Biostatistical Programmer (Contractor)
READING, ENGLAND, UNITED KINGDOM
...experience within clinical trials. Experience with computerised information systems is preferred. Familiarity with ICH and local regulatory authority regulations in drug research and development is advantageous. Proficient in Microsoft Office applications, with a strong understanding of data...
Sr Site Enablement Solutions Project Lead
64709
READING, LONDON (GREATER), READING, LONDON (GREATER)
Role Overview: 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, patient visits...
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...
Clinical Trial Manager - Virology - Inside IR35
LONDON, SOUTH EAST ENGLAND
p b Job Title: /b Clinical Trial Manager - Virology br b Location: /b West London br b Employment Type: /b Contract br b Duration: /b 12 months initial (possible extension) br b Schedule: /b 3 days on-site, 2 days remote /p p b Overview: br /b Join a leading Biotechnology firm in West...
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