Freelance Clinical Research Associate
... jeopardize the conduct of the clinical projects assigned. Reports to the Head of Clinical Monitoring Unit on all activities performed during the study and sends all relevant documents ...
... jeopardize the conduct of the clinical projects assigned. Reports to the Head of Clinical Monitoring Unit on all activities performed during the study and sends all relevant documents ...
... , CRFs and other study specific materials to and from the clinical sites. Perform investigational product inventory ... May review protocols, eCRFs, study manuals and other study related documents, as requested by the Clinical Trial Manager. May conduct on- ...
... Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project ... Oncology or equivalent) with sound clinical oncology experience and (ideally) some ... of Basic Science and or Clinical Research Sound medical and scientific ...
... Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project ... Oncology or equivalent) with sound clinical oncology experience and (ideally) some ... of Basic Science and or Clinical Research Sound medical and scientific ...
... -specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors ...
... Coordinator to join our vibrant Clinical Operations team in Munich. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic ...
... and ethical standards of the study. Work closely with clinical, regulatory, and project management teams to ensure Good Clinical Practice (GCP) and regulatory compliance. ...
... , science, or equivalent Experience in clinical trials (IHCRA, CTA or Study Coordinator) Knowledge of ICH-GCP ...
... opportunity for you Our successful Clinical Research Associates possess varied backgrounds ... - MEDPACE CRA TRAINING PROGRAM No clinical experience is needed as Medpace ... may also participate in other clinical research departmental core rotations, learning ...
... site staff including coordinators, clinical research physicians and their site ... with the protocol; Assessing the clinical research site’s patient recruitment and ... record of demonstrating experience in clinical patient management, protocol, CRF, preparing ...