- SUNY Upstate Medical University (Syracuse, NY)
- …of education and experience. SoCRA certified or ACRP certified Experience with clinical research protocols, knowledge of medical terminology, computer skills, ... for the clinical trial. Manage all aspects of the clinical trial at the Sponsor Level including but not limited to: Procuring study drug, site selection… more
- Guthrie (Sayre, PA)
- Position Summary: Coordinate multiple in-patient and out-patient clinical research protocols. Education/Experience: Required: An Associate 's degree in ... experience with study coordination, and documented training of good clinical research standards training preferred. The completion...IRB, and event management of patient follow-up visits. Submit research data to sponsor via the appropriate… more
- Cedars-Sinai (Los Angeles, CA)
- …year of experience as a clinical research coordinator or clinical research associate /assistant preferred. + Demonstrated ability to accurately ... team and contribute to groundbreaking research .** This position functions as a Clinical Research Coordinator providing support for clinical research … more
- Georgetown Univerisity (Washington, DC)
- …(eg, the study monitor appointed by the sponsor for each trial). The Associate Director and the Director of Clinical Trials rely on timely responses from ... to making a difference in the world. Requirements The Clinical Research Coordinator 2 (CRC2) is responsible...a daily basis, the CRC2 will report to the Associate Director of Clinical Trials. The CRC2...to the sponsor contact… more
- SUNY Upstate Medical University (Syracuse, NY)
- … trial. Duties include but are not limited to: coordinate all aspects of the clinical trial at the Sponsor Level including but not limited to: procuring study ... This role will act as the project manager for a large multi-site clinical trial where the clinical site is also the coordination center for the clinical… more
- University of Michigan (Ann Arbor, MI)
- Clinical Research Assistant Apply Now **How to Apply** A cover letter is required for consideration for this position and should be attached as the first page of ... relate to this position. **Job Summary** The Program for Clinical Research in Dermatology (PCRiD) is seeking...accurately with quality and in a timely fashion per sponsor requirements. May require data entry into both electronic… more
- Hartford HealthCare (Hartford, CT)
- …disability status.* ** **Job:** **Health Professionals* **Organization:** **Hartford Hospital* **Title:** * Clinical Research Assistant - Clinical Research ... Helps maintains adequate inventory of study supplies. Follows the sponsor protocol and Research Administration's policies on...Associate degree, four plus (4 ) years of research experience will be considered. At least one-year practical… more
- Rush University Medical Center (Chicago, IL)
- …strongly preferred (Certified Clinical Research Professionals (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical ... vary depending on the circumstances of each case. This Clinical Research Coordinator position will reflect duties...summary report(s) for distribution to PI, Administrator, Office of Research Affairs, Sponsor and Compliance throughout the… more
- Rush University Medical Center (Chicago, IL)
- …**Certifications:** * Certified Clinical Research Professionals (CCRP), * Certified Clinical Research Associate (CCRA), * Certified Clinical ... may vary depending on the circumstances of each case. **Summary:** The Clinical Research Coordinator II (CRC II) independently coordinates assigned aspects… more
- Rush University Medical Center (Chicago, IL)
- …certification as a Certified Clinical Research Professionals (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research ... of each case. **Summary:** This positions provides regulatory support for multiple clinical research studies, which may involve multi-centered cooperative group… more
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