- IQVIA (Durham, NC)
- …prior monitoring experience. * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice ... 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)
- **Position Summary** The Clinical Research Associate (CRA) will be responsible for designing, planning, coordinating, and conducting all activities involved ... Skills and Knowledge Requirements** + ≥2 years of experience as a Clinical Research Associate , with specific in vitro diagnostics study experience +… 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
- 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
- Stony Brook University (Stony Brook, NY)
- Clinical Research Associate II **Required Qualifications (as evidenced by an attached resume):** Bachelor's degree (foreign equivalent or higher). Three (3) ... Sponsor forms in accordance with GCP timelines. Oversees research equipment and study supplies. + Maintain knowledge and...of posting.** **Job Number:** 2503889 **Official Job Title:** : Clinical Research Associate II **Job… 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
- Stony Brook University (Stony Brook, NY)
- Clinical Research Associate I (Per Diem) **Required Qualifications (as evidenced by an attached resume):** Bachelor's degree (foreign equivalent or higher) ... database. Experience working with study participants. **Brief description of duties:** The Clinical Research Associate will assist with research… 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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