- Lovelace Biomedical Research Institute (Albuquerque, NM)
- OverviewA Research Coordinator position is currently available in Dr. Kent Kiehl's laboratory at The Mind Research Network in Albuquerque, New Mexico.The research ... coordinator will work with a team on grant-funded studies...(eg, psychopathic) traits, substance use disorders, and/or past traumatic events (including traumatic brain injury). Our studies also investigate… more
- University of Southern California (Los Angeles, CA)
- Protocol Coordinator (Research Nurse)Apply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Protocol - ... strong interest in clinical research. The role of the protocol coordinator is a diverse one. This...their regulations, especially concerning the reporting of Serious Adverse Events . Enters SAE into iStar for reporting to the… more
- Guidehouse (Baltimore, MD)
- …Trust **What You Will Do** **:** We are currently searching for Clinical Protocol Coordinator to provide support services to satisfy the overall operational ... staff to coordinate amendments, annual reviews, triennial reviews, terminations, adverse events , and other IRB interactions. + Facilitate communication with IRB and… more
- Joint Activities (Miami, FL)
- Summary About the Position: The incumbent will serve as a Protocol and Events Coordinator at USSOUTHCOM-Chief of Staff-Joint Engagement Visitors Bureau in ... Miami, FL. Responsibilities Serve as the Protocol and Events Coordinator for...transportation of dignitaries to avoid any scheduling conflicts with event presentations; and 3). Track confirmation of responses from… more
- Guidehouse (Bethesda, MD)
- …and participants enrolled in a National Institute of Allergy and Infectious Diseases protocol . The Patient Care Coordinator (PCC) will be responsible for all ... **Job Family** **:** Patient Care Coordinator (Digital) **Travel Required** **:** None **Clearance Required** **:** Ability to Obtain Public Trust **What You Will… more
- ATSG Corporation (Washington, DC)
- …meeting coordination, and/or program management or minimum three (3) years as a protocol affairs specialist/special events coordinator in private industry. + ... FBI Program Analyst III (IMMEDIATE HIRE) - International Protocol Unit (IPU) Washington, DC . Administrative Apply...FBI Legat. + Organize, plan, and prioritize meetings and events and assist with FBI larger conference planning. +… more
- University of Pennsylvania (Philadelphia, PA)
- …study period. Will record and report adverse events and serious adverse events per protocols. Manage patient treatment per protocol , schedule clinical and ... programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Department of Pulmonary, Allergy and Critical Care) Job Profile Title… more
- University of Pennsylvania (Philadelphia, PA)
- …must be documented in PennChart. The CRC will be responsible for gather the data per the protocol and bring any adverse events to the attention of the PI or any ... resources, and much more. Posted Job Title Clinical Research Coordinator A/B (Department of Cardiovascular Surgery) Job Profile Title...will be responsible for gather the data per the protocol and bring any adverse events to… more
- Johns Hopkins University (Baltimore, MD)
- …the IRB initial application, annual IRB continuing reviews, changes in research, protocol amendments, annual reports and events reports according to IRB ... by research protocols according to DOT/IATA regulations. + Maintain regulatory binders per protocol . + Document adverse events and protocol deviations. +… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title Clinical Research Coordinator B Job ... the University of Pennsylvania is actively seeking a dedicated, full-time Clinical Research Coordinator to join our team. This pivotal role will support and manage a… more
- Actalent (Gardena, CA)
- …+ Resolve all queries, manage and report adverse events , serious adverse events , and deviations, implement new protocol amendments, and provide all close-out ... Job Title: Clinical Research Coordinator II (Gardena)Job Description The Clinical Research ...start-up through study close-out in accordance with the study protocol , GCP, and SOPs. This role involves implementing and… more
- University of Southern California (Los Angeles, CA)
- …Coordinator IApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/Research- Coordinator -I\_REQ20157582-1/apply) ... interest in clinical research. The role of the Research Coordinator I is a diverse one. This person works...those listed below. Specific Job Functions I. Research A. Protocol Related 1. On request from supervisor, reviews in-house… more
- Johns Hopkins University (Baltimore, MD)
- …with clinical trial financial management staff to identify procedures, laboratory tests and protocol events that require invoicing to the Sponsor as defined in ... Research Program Manager or the Principal Investigator. The Sr. Research Program Coordinator is responsible for monitoring the clinical course and collection of… more
- HCA Healthcare (San Antonio, TX)
- …and other supplies as needed 3. Reports and follows up on serious adverse events as per the protocol and regulations 4. Implements study-specific communications ... requirements according to site work instructions/SOPs 6. Tracks and reports adverse events , serious adverse events , protocol waivers, and deviations 7.… more
- University of Pennsylvania (Philadelphia, PA)
- …and devices. The coordinator will execute and ensure adherence to the protocol and Good Clinical Practice, while taking an active role in preparation of trial ... resources, and much more. Posted Job Title Clinical Research Coordinator C (Department of Cardiovascular Medicine) Job Profile Title...study. Notify PI, managers, sponsor of any deviations from protocol or adverse events . Assure reported trial… more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Abramson Cancer Center) Job Profile Title Clinical Research Coordinator ... ACC. The ACC CRU Airways Research Team seeks a full-time Clinical Research Coordinator to organize, coordinate and implement complex cancer studies involving a wide… more
- CommonSpirit Health (Carmichael, CA)
- …protocols. + Identify and report all unanticipated and other adverse/serious adverse events , as well as protocol deviations, violations or exceptions, to ... study. Under the direction of the MCRM and/or Senior Clinical Research Coordinator , the incumbent assists with clinical trial or other research project coordination… more
- Johns Hopkins University (Baltimore, MD)
- …with clinical trial financial management staff to identify procedures, laboratory tests and protocol events that require invoicing to the Sponsor as defined in ... Radiation Sciences and JHU and participating sites. The Sr. Research Program Coordinator is responsible for the organization, entry, maintenance and accuracy of all… more
- University of Pennsylvania (Philadelphia, PA)
- …and assessing potential treatments for Williams Syndrome. Clinical Research Coordinator work includes study design, protocol development, submission ... visits and regulatory compliance in one or more studies. Clinical Research Coordinator work includes study design, protocol development, submission to review… more
- Hackensack Meridian Health (Edison, NJ)
- …that all protocol revisions, informed consents, continuing reviews, serious adverse events are submitted to the appropriate IRB of record in a timely manner. ... investigator in the preparation of proposed clinical trials by reviewing trial protocol , contacting each department who will provide resources during study and… more
