- Rush University Medical Center (Chicago, IL)
- …the circumstances of each case. **Summary:** This position handles the more complex clinical research studies conducted by PI(s) which may include grant-funded, ... industry sponsored, and investigator-initiated clinical research studies . Partners with the PI...(CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB… more
- Rush University Medical Center (Chicago, IL)
- …position. Offers may vary depending on the circumstances of each case. This Clinical Research Coordinator position will reflect duties in Neuroscience and ... (GCP) .S/he will coordinate and manage multiple and/or complex clinical research studies conducted by PI(s) which...timely manner. * Submits or partners with a regulatory coordinator to submit study related documents, … more
- University of Pennsylvania (Philadelphia, PA)
- …wealth of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical Research ... and industry initiated, different disease states and varying complexities. Research coordinator work includes study design, protocol development, submission to… more
- Rush University Medical Center (Chicago, IL)
- …Professional (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professionals (CIP) ... the study coordinators to ensure all aspects of complex studies , including recruitment, consent, screening, scheduling, and tracking and provides study… more
- University of Pennsylvania (Philadelphia, PA)
- … meetings. Job Description Job Responsibilities . Coordinate and conduct clinical studies , includes; subject recruitment, informed consent, chart maintenance ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator A Job Profile Title...federal regulations and guidance documents for the conduct of clinical studies and human subject protection .… more
- Dana-Farber Cancer Institute (Milford, MA)
- …protocol eligibility, obtain informed consent (minimal risk studies ), and register study participants to clinical trials. Travel to the Longwood campus and ... and regulatory documents as it pertains to participation in clinical trials across all studies open at...IRB submissions as it pertains to the regional campus' studies . Maintain and organize study regulatory binders,… more
- Stanford University (Stanford, CA)
- …in Precision Psychiatry and Neuroimaging to execute precision medicine in mental health studies , The Clinical Research Coordinator Associate in Precision ... Clinical Research Coordinator Associate **School of... Associate (CRCA) position is on a precision medicine study of depression funded by NIH under an exciting… more
- Beth Israel Lahey Health (Burlington, MA)
- …administration of multiple research studies . Responsible for assigned research studies and general research duties. Implements study protocols in accordance ... research staff and Research Administration facilitating all aspects of assigned clinical trials. Interacts with study participants diagnosed with various… more
- Rush University Medical Center (Chicago, IL)
- …Offers may vary depending on the circumstances of each case. The Associate Clinical Research Coordinator will provide support and contribute to a neuroscience ... Clinical Practice (GCP) S/he will coordinate standard clinical research studies conducted by PI(s) which...and procedures. **Required Job Qualifications:** * Bachelor's degree and 1 year of clinical research experience OR… more
- Avera (Pierre, SD)
- …upon experience._ $20.50 - $36.50 **Position Highlights** We are looking for a ** Clinical Research Coordinator ** or **Research Assistant** On-Site in Pierre, SD. ... listed below. **Research Assistant:** High School Diploma or GED ** Clinical Research Coordinator :** Clinical Research...the community. **What you will do** + Coordinates research studies per Good Clinical Practices guidelines, FDA… more
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