- Stanford University (Stanford, CA)
- …seeks a board-certified or eligible Breast Medical Oncologist as Assistant Professor, Associate Professor, or Full Professor in the University Medical Line (UML). An ... or eligible in medical oncology. The candidate should have training as an investigator with a track record of research funding and a strong publication record,… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Jun 10, 2025 Requisition # 106623 The Clinical ... Research Coordinator Associate is responsible for the overall management and implementation...finance and/or management staff. + Interact with the principal investigator regularly, ensuring patient safety and adherence to proper… more
- Cedars-Sinai (Los Angeles, CA)
- …and women's health. You can continue your career journey with us! **Principal Investigator , Paul Noble, MD invites you to consider this great opportunity to join ... pulmonary disease related to connective tissue disease. The Research Associate I will perform a variety of routine experimental...most. **Req ID** : 8988 **Working Title** : Research Associate I - Noble Lab - Lung Institute /… more
- IQVIA (Carlsbad, CA)
- …faster._ **Job Overview** We are seeking a detail-oriented and proactive Clinical Research Associate (CRA) to join our team. In this role, you will be responsible ... is properly maintained and filed in the Trial Master File (TMF) and Investigator Site File (ISF) per GCP and local regulations. + Document site interactions… more
- Translational Research in Oncology (Los Angeles, CA)
- If you are an experienced Clinical Research Associate who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is ... storage, dispensation, tracking and accountability, and destruction/return) + Perform Investigator Study File reconciliation: request any new or updated site-related… more
- Cordis (Irvine, CA)
- …that address unmet and critical medical needs. **Responsibilities** The **Clinical Research Associate (Coronary)** role is a key position within the coronary program ... a high quality + Assist with organization and content preparation for Investigator meetings and Study Coordinator meetings + Ensure proper escalation of site/project… more
- BeOne Medicines (Emeryville, CA)
- …deep understanding of cost structure for each spend category, including the investigator grant, Central labs, IVRS, Imaging, SMO, patient recruitment, Comparator and ... Clinical Depot, etc. + Manages the identification and selection process of clinical vendors. + Generates Requests for Information (RFI) and Requests for Proposals and budget grids. + Coordinates bid defenses and proposal review meetings and provides analysis… more
- IQVIA (Carlsbad, CA)
- …available for filing in the Trial Master File (TMF) and verify that the Investigator 's Site File (ISF) is maintained in accordance with GCP and local regulatory ... requirements. * Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. * Collaborate and… more
- Abbott (Alameda, CA)
- …Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and ... training of new study investigators and writing and assembling submissions. + Maintain and audit Trial Master File to ensure inspection readiness. + Perform review of clinical data listings for completeness and accuracy, and escalate issues to the Clinical… more
- IQVIA (Carlsbad, CA)
- …are available for filing in the Trial Master File (TMF) and verify that the Investigator 's Site File (ISF) is maintained in accordance with GCP / ICH and local ... regulatory requirements. * Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. * Act as a… more
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