- Houston Methodist (Houston, TX)
- …accurate regulatory filing. + Assists Clinical Trial Manager in identifying opportunities research workflow process improvement, providing ... multiple projects under supervision of Clinical Trial Manager which may include clinical research protocols, gathering patient data via methods… more
- Arkansas Children's (Little Rock, AR)
- …Understanding the long-term impact of COVID on children and families **Summary:** The Clinical Research Professional I coordinates selected specific aspects of ... clinical research studies. This...Maintains files and study documentation according to institutional and regulatory standards 8. Performs other duties as assigned. Arkansas… more
- Northern Light Health (Brewer, ME)
- …for possible entry into clinical trial. Supports the safety of clinical research patients/ research participants Coordinates protocol related research ... Reports adverse events Understands and is compliant with good clinical practice (GCP) and regulatory compliance with...and other tools to support the studies with the research manager May represent the interests of… more
- Guthrie (Sayre, PA)
- Position Summary: Coordinate multiple in-patient and out-patient clinical research protocols. Education/Experience: Required: An Associate's degree in applied ... , documented experience with study coordination, and documented training of good clinical research standards training preferred. The completion of the CITI… more
- Dayton Children's Hospital (Dayton, OH)
- … clinical research activities under the general direction of the Clinical Research Supervisor/ Manager and a Principal Investigator (PI) while adhering ... submissions and regulatory processes. Most important of all, the Clinical Research Coordinator will ensure the safety and well-being of all study… more
- Cordis (Irvine, CA)
- …imaging collections, regulatory requirements. The CRA will ensure relevant clinical research guidelines are adhered to and that project timelines ... The Clinical Research Associate (CRA) reports to the Clinical Monitoring Manager . The CRA is responsible for the initiation, maintenance… more
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title Clinical Research ... Coordinator B Job Description Summary The Clinical Research Coordinator is responsible for oversight, execution, and regulatory compliance of human subject … more
- Terumo Neuro (Aliso Viejo, CA)
- **12869BR** **Title:** Clinical Research Assoc, Sr. **Job Description:** Responsible for coordinating clinical research activities in accordance with ICH ... address and resolve queries. + Work closely with Project Manager (s) to ensure clinical studies are conducted...related field. 2. Minimum six (6) years of direct clinical research experience, preferably in the medical… more
- Avania (OR)
- Avania are hiring for the key role of experienced Clinical Research Associate (CRA) or Senior Clinical Research Associate (Sr CRA) As a CRA/Sr CRA you ... for several studies running in parallel, in all associated clinical trial phases, from regulatory submissions to...3 + years of relevant work experience as a clinical research associate - CRA. + Attention… more
- ConvaTec (VA)
- …(LSE:CTEC). To learn more please visit http://www.convatecgroup.com **About the role** The Clinical Research Associate (CRA) ensures the effective and efficient ... and communicates monitoring issues and risks to the Convatec Clinical Study Manager . The CRA ensures the...to properly assess an investigative site's capabilities for conducting clinical research . Knowledge of how to select… more
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