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Patient Safety Specialist
LONDON, GB
Patient Safety Specialist London-Hybrid on site 3 days Contract Length: 12 months Maternity cover Job Purpose: To support management of Patient Safety operational processes at the country organization, ensuring compliance with global and local procedures, national and international regulations...
Clinical Trial Specialist
, , UNITED KINGDOM
...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...
Research Scientist (Agriculture)
£30,000
DAVENTRY
Research Scientist/trials manager required for role in Northamptonshire with background in agronomy or a related field Research Scientist (Agriculture) Northamptonshire (commutable from Northampton, Daventry, Rugby, Coventry and surrounding areas) - Driving license required Salary - £30,000...
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Research Scientist - Clinical Trials
TRURO, CORNWALL, CORNWALL; SOUTH WEST ENGLAND; ENGLAND, UK
This is a fantastic opportunity in Cornwall to act as a Principal Clinical Scientist (radiotherapy) for the service delivery of radiotherapy physics support. You will be joining a thriving department possessing two Varian TrueBeam linear accelerators with 6 degrees of freedom couches, Xstrahl...
Senior Clinical Quality Assurance Specialist (Remote / Home Based)
OXFORD, ENGLAND, GB
...follow-up independent clinical quality assurance audits including associated quality management activities and provide input into the audit schedule. Acts as Lead auditor as applicable. To support Clinical Quality Assurance in its application and development of the Quality Management System and...
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Clinical Research Specialist
SOUTH PLAINFIELD, NJ, UNITED STATES
Responsibilities: Site Management experience (site or sponsor). Knowledge of/experience with CTMS/EDC/TMF. Experience with Good Clinical Practice (GCP). Oversees, designs, plans, and develops clinical evaluation research studies. Prepares and authors protocols and patient...
Clinical Trial Specialist
MAIDENHEAD
...affairs within clinical trials. /p p strong Responsibilities: /strong /p p • 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...
Graduate Trainee
TWICKENHAM, , UNITED KINGDOM
...more!Our people are specialists in leading research funding on behalf of organisations for the benefit of wider society. The Grant Management Group delivers research management, communications and engagement and provides expertise in the funding and management of commercial and technological...
Emergency Medicine, Speciality Doctor
CANTERBURY, ENGLAND, UNITED KINGDOM
...to patients including clinical leadership and supervision of junior medical staff, ensuring the highest standards of clinical care are provided to all patients attending the ED. To be proactive in ensuring that all patients receive rapid assessment, treatment and clinical decision making...
Regulatory Specialist
MAIDENHEAD, UNITED KINGDOM
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote.The Role:The Regulatory Associate is responsible for providing global...
Cardiac Physiologist for Invasive Cardiology
LONDON, GB
...should have advanced clinical knowledge in Electrophysiology and CRM. This will be balanced with some Interventional Cardiac procedures. A renewal, refresh training on Interventional Cardiology can be provided to the candidate who already possesses previous experience and core knowledge...
Head of Clinical Development
BOSTON, GB
Hobson Prior is seeking a dynamic and accomplished professional for the role of Head of Clinical Development. This role involves leading and managing the clinical development team, providing strategic guidance, and overseeing clinical trial data. The ideal candidate will have a strong background in...
Associate Director Clinical Data Management, Oncology - UK
CITY OF LONDON, GB
Proclinical is seeking a dedicated individual for the role of Associate Director, Clinical Data Management. The successful candidate will be responsible for leading the team and overseeing the execution of clinical trials. Responsibilities: - Organise and conduct team meetings. - Foster team...
Director, Clinical Compliance (GCP)
CITY OF LONDON, GB
Proclinical is seeking a dedicated and proactive Director of Clinical Compliance. This role focuses on establishing and implementing a Quality Strategy for clinical development activities. The successful candidate will ensure all work is in agreement with regulatory requirements and will adherence...
Director, Clinical Quality Assurance
CITY OF LONDON, GB
Proclinical is seeking a dedicated and experienced Director of Clinical Quality. This role is pivotal in developing and implementing quality assurance strategies that support our clinical portfolio. The successful candidate will be responsible for establishing effective GCP QA audit programs and...
Principal Scientist (Translational)
LONDON, GB
Northreach is a dynamic talent solutions specialist that connects businesses with top talent in the cell & gene therapy, fintech, and digital sectors. Our mission is to provide a seamless and personalised recruitment experience for clients and candidates, and to create a positive work...
QA Officer
CAMBRIDGE, GB
Hobson Prior is seeking a Quality Assurance Specialist on a permanent basis. This role focuses on maintaining and improving the Quality Management System (QMS) whilst developing diagnostic capabilities. This includes supporting internal audits, assisting with client audits, and providing support...
Senior Statistician
LONDON, GB
...have experience in clinical research. You should have a strong understanding of statistical methods, the drug development process, and good programming practices. You should be familiar with CDISC standards. You should be able to plan, supervise, implement and monitor the statistical...
UK CW Regulatory Affairs Manager - remote
CITY OF LONDON, GB
...e.g. late stage clinical trials, variations, extensions and marketing applications) for products within company's portfolio in compliance with global filing plans and local regulatory requirements with minimal supervision. Authoring and coordinating responses to questions across assigned...
Development Chemist
22916
KETTERING
...on production trials Working to ensure claims have been substantiated Reviewing chemical ingredients regularly Requirements: Degree in Chemistry or Cosmetic Science Formulation experience in Biocides, Detergents or Cosmetics Experience managing projects from concept to commercialisation...
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