Clinical Trial Manager (CTM) jobs
Clinical Trial Manager (CTM) jobs involve overseeing and managing all aspects of clinical trials, from planning and initiation to execution and completion. CTMs are responsible for ensuring that clinical trials are conducted in compliance with regulatory requirements, protocol specifications, and Good Clinical Practice (GCP) guidelines. They collaborate with cross-functional teams, including investigators, study coordinators, data management personnel, and external vendors, to ensure the successful execution of clinical trials. CTMs are involved in study start-up activities, such as site selection, protocol development, and regulatory submissions, as well as monitoring study progress, addressing issues and risks, and managing study timelines and budgets. They also play a crucial role in ensuring the safety and well-being of trial participants and the quality and integrity of data collected. Strong project management skills, knowledge of clinical trial regulations, and excellent communication and leadership abilities are essential for CTMs in effectively overseeing clinical trials.
Found jobs - 114
Exact matches
Single Sponsor Local Study Manager/Clinical Trial Manager - UK home based (with occasional UK travel)Syneos - United Kingdom16 days old
Clinical Trial Manager - Germany - Neuroscience / OphthalmologyMedpace - Munich, GermanyPosted 30+ days ago
Associate Clinical Trial Manager (PhD) - Neuroscience / OphthalmologyMedpace - Munich, GermanyPosted 30+ days ago
Associate Clinical Trial Manager (PhD) - Infectious Disease / ImmunologyMedpace - Munich, GermanyPosted 30+ days ago
Clinical Trial Manager - Germany (Munich) - Infectious Disease / ImmunologyMedpace - Munich, Germany; London, United KingdomPosted 30+ days ago
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RTSM Project Manager (Randomisation and Trial Supply Management)GSK - Stevenage, United Kingdom5 days old
Single Sponsor Site Activation Specialist II (UK/Ireland Submissions) - Hybrid - 3 days in MaidenheadSyneos - City of London, United Kingdom9 days old
Manager, E.U. Medical Device & IVD RegulationJohnson & Johnson - Beerse, Belgium; High Wycombe, United Kingdom; Allschwil, Switzerland10 days old
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Principal Scientist (m/f/d) Pathology, 3 year fixed-termBoehringer Ingelheim - Vienna, Austria15 days old
Sponsor Dedicated Regulatory Portfolio Snr. Regulatory Consultant (GRO RPSM) open to Spain, Portugal and UK locationSyneos - Madrid, Spain15 days old
Sponsor Dedicated Regulatory Portfolio Snr. Regulatory Consultant (GRO RPSM) open to Spain, Portugal and UK locationSyneos - Barcelona, Spain15 days old
Sponsor Dedicated Regulatory Portfolio Snr. Regulatory Consultant (GRO RPSM) open to Spain, Portugal and UK locationSyneos - United Kingdom15 days old












