- IQVIA (Carlsbad, CA)
- IQVIA is seeking Study Start-Up Clinical Research Associates to join our Sponsor Dedicated teams. Ideal candidates will have experience in Study Start-Up and ... with the sponsor strategy IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life… more
- IQVIA (Carlsbad, CA)
- …in lieu of degree. Req * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- IQVIA (Parsippany, NJ)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- IQVIA (Philadelphia, PA)
- …and owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements ie ICH GCP and relevant local laws,… more
- Stony Brook University (Stony Brook, NY)
- Clinical Research Associate I **Required Qualifications (as evidenced by an attached resume):** Licensed Practical Nurse in the state of New York. Two (2) ... Clinical Research Coordinator (CCRC). **Brief Description of Duties:** The Clinical Research Associate I would be responsible for supporting the… more
- Rush University Medical Center (Chicago, IL)
- …disability, veteran status, and other legally protected characteristics. **Position** Associate Clinical Research Coordinator **Location** US:IL:Chicago ... works under the general direction of the Office of Research Affairs' Clinical Research Administration...and responds to questions from PI, Administrator, Office of Research Affairs, Sponsor and Compliance throughout the… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Sep 10, 2025 Requisition # 107255 ... The Stanford Stroke Center is seeking a Clinical Research Coordinator Associate to...databases, and regulatory files. + Participate in monitoring visits, sponsor meetings, and regulatory audits, serving as the study… more
- Parexel (Atlanta, GA)
- …for candidates based in the Midwest, West Coast, Northeast & North Carolina The Senior Clinical Research Associate (Sr. CRA) is responsible for the site ... local country regulations + Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) +… more
- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Oct 15, 2025 Requisition # 107524 ... Stanford University's Department of Neurosurgery is seeking a Clinical Research Coordinator Associate (CRCA)...**Duties Include*:** + Serve as the primary contact with research participants, sponsor , and regulatory agencies. +… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: The Clinical Research Associate I will be responsible for the coordination of clinical research studies within the Department of ... data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory, processing clinical trial billing… more
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