- University of Pennsylvania (Philadelphia, PA)
- …Basic understanding of research ethics and an interest in learning about IRB processes and human subject research regulations Clinical Research ... + Flexible, detail-oriented, and able to multitask effectively + Familiarity with IRB processes and human subject research regulations Position contingent upon… more
- Emory Healthcare/Emory University (Atlanta, GA)
- **Discover Your Career at Emory University** Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate ... area. This role is part of thePEACH II Program (https://med.emory.edu/departments/medicine/divisions/infectious-diseases/ research /peach/index.html) , a CDC-funded initiative focused on preventing healthcare-associated… more
- University of Pennsylvania (Philadelphia, PA)
- …statistical software package and submit protocol modifications and continuing reviews to the IRB as needed, perform literature review , and write reports and ... private employer in Philadelphia, is a world-renowned leader in education, research , and innovation. This historic, Ivy League school consistently ranks among… more
- University of Pennsylvania (Philadelphia, PA)
- …safety. A high degree of autonomy, leadership, and expertise in GCP and institutional policies is expected. QUALIFICATIONS: Clinical Research Coordinator B + ... team + Flexible, detail-oriented, and able to multitask effectively + Familiarity with IRB processes and human subject research regulations + Position contingent… more
- University of Pennsylvania (Philadelphia, PA)
- …private employer in Philadelphia, is a world-renowned leader in education, research , and innovation. This historic, Ivy League school consistently ranks among ... health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A Job Profile Title Clinical Research Coordinator A Job… more
- Vanderbilt University Medical Center (Nashville, TN)
- …clinical trials experience including protocol requirements, patient recruitment, and familiarity with Internal Review Board ( IRB ) applications. This is an on ... through Friday. . KEY RESPONSIBILITIES + With assistance, prepares and processes new IRB research proposals, amendments, continuing review applications and… more
- Johns Hopkins University (Baltimore, MD)
- …group/internal audits/monitoring. + Assists with development & review of institutional SOPs pertaining to performance of clinical research . + Maintains ... design to evaluate new protocols. + Applies knowledge of federal & local regulations when evaluating new protocols. +...response. + Assumes responsibility for specific QA activities for research teams (ie, participates in institutional QA… more
- University of Utah (Salt Lake City, UT)
- …and trial management practices align with institutional , sponsor, and federal requirements. In collaboration with investigators, clinical research study ... Rate Range** 39300 to 54807.38 **Close Date** 01/23/2026 **Priority Review Date (Note - Posting may close at any...Knowledge of Good Clinical Practices, FDA , HIPAA and IRB regulations; an understanding of research procedures;… more
- Loyola University Chicago (Chicago, IL)
- …progress reports, and assisting with audits and monitoring visits. + Coordinate with the IRB , data safety monitoring board ( DSMB ), and other regulatory ... Clinical Research Nurse Project Coordinator Thank you for your...benefits. + Document the consent process in compliance with IRB guidelines and GCP standards. + M- MILK Intervention… more
- WellSpan Health (York, PA)
- …credits. **Common Expectations:** + Is knowledgeable of and complies with institutional research policies, procedures and guidelines. With the oversight ... research patients. **Essential Functions:** + Participates in the review of research protocols and assesses the...and welfare of human subjects (ie, DHHS, FDA and IRB research regulations, HIPAA privacy and … more