Since 1984, the TIMI Study Group has been an Academic Research Organization dedicated to advancing the knowledge and care of patients suffering from cardiovascular disease and its risk factors. We have led a wide array of clinical trials, from phase I to phase IV, enrolling from less than 30 to more than 26,000 subjects, and with both industry and NIH support. Trials have been conducted in over 50 countries and at more than 5000 separate sites.
The Clinical Trial Coordinator is part of the trial operations team, tasked with ensuring that each project is completed in compliance with the trial protocol, good clinical practice, regulatory requirements, and to sponsor/TIMI standards. Working independently and under general supervision, the Clinical Trial Coordinator will support one or more clinical trials and will be responsible for assigned administrative day-to-day project activities.
Candidates for this position should have a strong interest in clinical research and clinical trials. This position would be ideal for those candidates interested in gaining significant experience in medical research and learning from experienced clinicians and clinical trialists. To that end, though not formally within the expected scope of the position, the successful candidate will be encouraged and supported in seeking educational opportunities and training.
Job duties may include, but are not limited to:
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