- The University of Chicago (Chicago, IL)
- …work in our dynamic and collaborative environment. Job Summary The Clinical Research Coordinator 2 (CRC2) is a specialized researcher working with the Principal ... complex clinical trials that may include national level and multi- institutional pharmaceutical. Responsibilities include, but are not limited to,... process and when and how to apply for IRB review . Understanding of the federal research… more
- Planned Parenthood (Minneapolis, MN)
- …supervision of the Research Manager. This position will focus on research study start-up, Institutional Review Board ( IRB ) submissions, study project ... Day-to-Day Responsibilities: Study Coordination and Reporting Independently develop and prepare Institutional Review Board applications, including completion… more
- Cedars Sinai (Beverly Hills, CA)
- …study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... Job Description Join our team! The Clinical Research Coordinator II works independently providing study coordination including...including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB… more
- Northwestern University (Chicago, IL)
- …local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board ( IRB ), Food & Drug Administration ... science or related; OR appropriate combination of education and experience and 2 years' research study or other relevant experience required; OR Successful… more
- Kaiser Permanente (Vallejo, CA)
- …Compliance on an ongoing basis. If applicable and with supervision, coordinate IRB communications (eg, new protocols, amendments, continuing review applications, ... Job Summary: The Clinical Trial Research Coordinator I (CTRC-I) is a novice level position...guidance from PI, assist with ensuring compliance with KPNC IRB Standard Operating Procedures (SOP) and document applications. Adhere… more
- Nuvance Health (Norwalk, CT)
- …patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... Clinical Research Coordinator , Norwalk, CT Full-time, 40 hours - 8:30...protocols, consent forms, and other required documents to the Institutional Review Board ( IRB… more
- The University of Pennsylvania (Philadelphia, PA)
- …Other duties and responsibilities as assigned Regulatory Responsibilities: Prepare and process all Institutional Review Board ( IRB ) documentation through ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator B (Department of Gastroenterology) Job Profile Title Clinical Research … more
- The University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... team members in retrieval and provision of documentation required for IRB submission/renewals in accordance with guidelines; continuing review , modification,… more
- Mount Sinai Hospital (New York, NY)
- …grant applications and documents and assists in protocol submissions (for eg, Institutional Review Board , Grants and Contracts Office). Responsibilities ... complex clinical research data; Assists in interpreting clinical research data. 2 . Coordinates the clinical assessments of the study subjects including but… more
- The University of Pennsylvania (Philadelphia, PA)
- …patient/participant information *Assisting or leading in the preparation and submission of IRB documents Coordinator A: Assist in the coordination of federally ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator A/B (Department of Neurology) Job Profile Title Clinical Research … more
- Alliance Clinical Network (West Hills, CA)
- … 2 + years' experience working as a Clinical Research Coordinator , preferred. Comprehensive knowledge of FDA, GCP & confidentiality. Exceptional attention ... to improving patient lives every day. SUMMARY: We are seeking a Sr Clinical Research Coordinator to join ACN and lead our clinical operations team at our Los Angeles… more
- Actalent (Indianapolis, IN)
- …Basic computer skills. Strong customer service skills. Teamwork skills. Must have 2 + years of Clinical Research Coordinator experience. Additional Skills & ... Job Title: Clinical Research Coordinator Job Description As a Clinical Research ...process laboratory specimens for shipment according to study protocols. Review laboratory and ancillary tests, reporting results to the… more
- University of Miami (Miami, FL)
- …Department of SCCC has an exciting opportunity for a Full Time Clinical Research Coordinator 2 to work Hybrid at the UHealth Medical campus in Miami, ... FL. CORE JOB SUMMARY The Clinical Research Coordinator 2 (A) serves as a mid-level clinical research professional that assists in the planning, coordinating,… more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Cancer Clinical Research Coordinator 2 - GI (Hybrid) **School...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more
- Georgetown Univerisity (Washington, DC)
- …shared dedication to making a difference in the world. Requirements The Clinical Research Coordinator 2 (CRC2) is responsible for managing and coordinating 7 out ... week on site for these trials as the only coordinator for migraine/headache trials at our center, working exclusively...team of 6 CTM/CRC II s (including the CRC2), 2 Associate Directors, the Director of Clinical Trials, and… more
- Rush University Medical Center (Chicago, IL)
- …10. May assist PI with aspects of grant proposals. 11. May assist with Institutional Review Board assignments such as initial study approval, amendments, ... depending on the circumstances of each case. **Summary:** The Epi Research Coordinator 2 coordinates moderately complex Epidemiological, Behavioral or Human… more
- University of Miami (Miami, FL)
- …and participant compensation/reimbursement records. + Prepares and submits annual continuing reviews to the Institutional Review Board ( IRB ). + Notifies ... Palmer Eye Institute, has an exciting full time job opportunity for a Clinical Research Coordinator 2 in Miami, Florida. The Clinical Research Coordinator … more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Clinical Research Coordinator 2 (Fixed-term 12 months) **School...applications are submitted to the FDA when applicable. Ensure Institutional Review Board renewals are… more
- University of Miami (Miami, FL)
- …of Miami Health System, "UHealth" has an exciting opportunity for a Full-Time Clinical Research Coordinator 2 to work in the Peggy and Harold Katz Family Drug ... Discovery Center. The Clinical Research Coordinator 2 serves as a mid-level clinical...to approved protocols, help with study-related administrative tasks, facilitate across-the- board flow of information, and coordinate study activities and… more
- University of Miami (Miami, FL)
- …this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . The Clinical Research Coordinator 2 serves as a mid-level ... monitoring, and evaluating of specific clinical research studies. The Clinical Research Coordinator 2 will work within the Division of Digestive Health… more
