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Clinical trials specialist quality jobs

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Principal Regulatory Medical Writer £50,000 - £58,000 per annum LONDON ...and precision medicine clinical trials in oncology agents. Our broad portfolio rivals that of a medium-sized pharmaceutical company, spanning antibodies, cell therapies, vaccines, drug conjugates and small molecules, making this an interesting and dynamic area to work in. /p br br p strong...
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...
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...
Looking for Clinical Trials Specialist Quality jobs? Top Salaries! Full time, part time and contract. Visit PerfectJobs4U UK for the widest selection of top UK jobs. Full time, part time and work from home roles.
Associate Director - Quality Assurance LONDON, ENGLAND, UNITED KINGDOM ...high level specialist expertise to both the A team and key stakeholders in relation to this manufacturing site. The role has responsibility for building and managing a small team of A professionals and creating a strong quality culture on the site. The individual will deputise for...
Chief Executive Officer of the Royal Free Hospital Competetive LONDON, UNITED KINGDOM ...the development and clinical trials of the vaccines for COVID-19. We are a major teaching and research centre and one of the major partners of UCL university and deliver nationally and internationally renowned specialist clinical services alongside a wide range of local core services. The...
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Quality Team Lead LEICESTER, MIDLANDS p Are you experienced in GMP, with a quality background and people management experience? We have a Quality Team Lead opportunity within the Quality team here at Myonex. This is a role leading a GMP team to label and pack product for clinical trials, as well as work cross-functionally to support...
Clinical Trial Manager - Global Pharma - Complex Trials UNITED KINGDOM, , UNITED KINGDOM Title: Clinical Trial Manager - Global Pharma - Complex Trials Location: London Duration: Full Time Salary: Competitive Based on Experience We re very excited to be partnering with a Global Pharma who are seeking a Clinical Trial Manager, due to a expanding pipeline within Virology development. You...
Quality Team Lead LEICESTER, ENGLAND, UNITED KINGDOM Are you experienced in GMP, with a quality background and people management experience? We have a Quality Team Lead opportunity within the Quality team here at Myonex. This is a role leading a GMP team to label and pack product for clinical trials, as well as work cross-functionally to support...
Senior Clinical Quality Assurance Specialist , , UNITED KINGDOM ...looking for a Senior Quality Assurance Specialist to join their team. This successful candidate will be reporting to the Senior Clinical Quality Assurance Manager coordinate the implementation of the company quality management system relevant to GCP (including laboratory analysis of clinical...
Senior Quality Assurance Specialist LONDON AREA, UNITED KINGDOM, UNITED KINGDOM Myself and BioTalent have partnered up with a pioneering biotechnology company focused on developing novel cell and gene therapies, on their search for a Senior Clinical QA Specialist based at their London site. As a Senior Clinical QA Specialist you will be responsible for ensuring the integrity...
Head of Regulatory Affairs UNITED KINGDOM, , UNITED KINGDOM ...enhancing treatment and clinical results for patients living with cancer. Our client is seeking a dynamic leader to provide strategic input and leadership to project teams in support of developmental through to post-approval commitments. Discover more about our Head of Regulatory Affairs...
GCP QA Manager OXFORDSHIRE, ENGLAND, UNITED KINGDOM We are currently working with a pharma organisation who are a growing ecosystem of drug development companies, that provide integrated and specialist operational support for rapidly scaling biotech ventures. They are looking for a GCP QA Manager who will work closely with the Head of Quality and...
External Data Manager UNITED KINGDOM, , UNITED KINGDOM ...development strategy / clinical trial / and data management processes. Previous experience in a data management role. Understanding of different types of data sources within clinical trials. Ability to drive decision making and influence study teams. This role will see you work on a global scale...
Senior Statistician, Oncology (Remote) LONDON, ENGLAND, UNITED KINGDOM ...and to the required quality. Key Responsibilities Provide input on protocols such as study design, sample size calculations, and patient randomization schemes. Handle statistical aspects of case report form design. Review study database structures, edit checks, and data management coding...
Regional Sales Manager - Medical ST ALBANS, ENGLAND, UNITED KINGDOM Innovative global manufacturer with great product pipeline Premium quality products assisting NHS sustainability objectives. Strategic role with a C-Suite focus. Well-known brand Southeast Uncapped earning potential. Hybrid role with sales & managerial opportunity. Over 50 years...
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...
Senior Site Activation Specialist (contract negotiator) 37623 WARSAW, , WARSAW, Senior Site Activation Coordinator (Contract Negotiator) Country Site Activation Join us on our exciting journey IQVIA s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective...
Senior Specialist, CPSO Drug Product Dispensary Operations 40370 NEW BRUNSWICK, NEW JERSEY, UNITED STATES OF AMERICA, , NEW BRUNSWICK, NEW JERSEY, UNITED STATES OF AMERICA, ...working-with-us . Our Clinical Supply Operations is responsible for the supply of drug product administered to patients in clinical studies worldwide. In Global Product Development and Supply the team works closely with our partners to deliver quality products safely, efficiently and on time...
TMF Lead II (office-based) 48840 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...
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...
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