Research Coordinator II (7811)
The Office of Surgical Research within the Michael E. DeBakey Department of Surgery is seeking a skilled Research Coordinator (Level II) to coordinate day-to-day activities of research protocols which include screening, enrollment, and monitoring research participants. The coordinator will ensure accurate data collection, documentation, organization, and the safety of research participants. He/She will be responsible for ensuring accurate data collection, documentation, organization, and the safety of research participants. Additionally, the coordinator will assist with data collection, database management, and data analyses to identify and rank individual-level risk factors. The ideal candidate should be able to work well independently, have strong organizational skills, and working knowledge of medical terminology.
Coordinates day to day activities of research protocols which include screening, enrollment, and monitoring of research participants. Ensures accurate data collection, documentation, organization and safety of research participants.
Works with the Principal Investigator (PI) to assure that the study complies with all terms and conditions, including but not limited to education, IRB approval, conflict of interest disclosure, health and safety protections for participants and staff, and any financial terms or conditions. 15%
Collects patient information; processes documents and enters information into a database. Ensures accurate data collection, documentation, organization and safety of research participants.15%
Interviews, screen and recruits’ patients for study; explains process and procedures to educate participant regarding the research study.15%
May collect, process, ship, and maintain paperwork for blood and/or biological specimens according to procedures outlined in study protocol. 10%
Maintains records and regulatory documents and records for research studies.10%
Schedules research participant for tests and procedures such as laboratory tests, x-rays, and other studies specific for the research protocol. 10%
Retrieves and submits test results to appropriate party. 5%
Assists the Principal Investigator in the submission of event reports, including but not limited to Non-compliance, Adverse Events, and Unanticipated Problems. 5%
Keeps track of Protocol Amendments, Clarification letters and study updates and implement updates accordingly. 5%
Attends investigator meetings as required or requested by the PI and/or Sponsor. 5%
Responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, and the Principal Investigator.
Will be responsible for enrolling research subjects in clinical and hospital settings.
Will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials.
Will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols.
Bachelor's degree in a related field. Four years of related experience may substitute for degree requirement.
One year of relevant experience.
Current certification (Certified Clinical Research Professional-CCRP, Certified Clinical Research Coordinator-CCRC) from a clinical research organization (SoCRA or ACRP).
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.
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