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Clinical trials specialist project 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...
Regulatory Clinical Trials Submission Manager UNITED KINGDOM, , UNITED KINGDOM ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions...
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...
Looking for Clinical Trials Specialist Project 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.
Regulatory Clinical Trials Submission Manager UNITED KINGDOM, UNITED KINGDOM p ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research...
Senior Clinical Quality Assurance Specialist , , UNITED KINGDOM ...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 samples) including...
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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...
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...
Director Regulatory Affairs , , UNITED KINGDOM ...input and leadership to project teams in support of developmental and post-approval projects. Discover more about our Regulatory Affairs Director opportunity its objectives, duties/responsibilities and the skills, experience and competencies needed to succeed. Your objectives: As the Regulatory...
Key Account Manager UNITED KINGDOM, , UNITED KINGDOM Company Overview: Join our client a specialist pharmaceutical supply business dedicated to advancing healthcare through innovative services. Who are seeking a Remote Key Account Manager based in the UK to support their growing client base. Position Overview: As a Key Account Manager, you'll manage...
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...
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...
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...
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...
Senior Clinical Quality Assurance Specialist UNITED KINGDOM, UNITED KINGDOM ...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 samples) including...
Head of Clinical Engineering and Sterile Services £80 - 100 STEVENAGE We are recruiting for a Head of Clinical Engineering and Sterile Services who shares our vision to be trusted to provide consistently outstanding care and exemplary service to our patients. br br Experience, qualification, and soft skills, have you got everything required to succeed in this...
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...
Head of Regulatory Affairs UNITED KINGDOM, UNITED KINGDOM ...enhancing treatment and clinical results for patients living with cancer. /p p br /p p 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. /p p br /p p Discover more about our...
Senior Account Executive £60 - 80 LONDON ...communication specialists across the disciplines of medical education and communications; brain sciences; brand promotion; digital and social; strategic planning; public relations and creative/design. br b About the Role /b /p br p We have a fantastic opportunity for a Senior...
Senior Account Executive £60 - 80 LONDON ...communication specialists across the disciplines of medical education and communications; brain sciences; brand promotion; digital and social; strategic planning; public relations and creative/design. /p br About the Role br p We have a fantastic opportunity for a Senior Account...
Director Regulatory Affairs UNITED KINGDOM, UNITED KINGDOM ...input and leadership to project teams in support of developmental and post-approval projects. /p p br /p p Discover more about our Regulatory Affairs Director opportunity; its objectives, duties/responsibilities and the skills, experience and competencies needed to succeed. /p p br /p p b...
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