Clinical Research Nurse Coordinator/ Project Coordinator
5 days ago
Job Description/Summary:
This is a temporary position as the Clinical Research Nurse Coordinator (CRNC)/ Project Coordinator for an NIH-funded research study in the Houston Medical Center. This study is looking at the effects of a therapeutic intervention during pregnancy for Hispanic and African American women, hoping to improve maternal mental health and infant outcomes. The CRNC will manage the day-to-day activities of the study in coordination with the Clinical Research Associate (CRA) and report to the Principal Investigator (PI).
Job Hours:
This position will be needed from April 2025- June 2025. Any needed training will take place the last two weeks of March 2025. You will be needed 2-4 days/week (depending on workload and availability) Monday-Friday during regular business hours. There are no weekends, holidays or nights needed.
Position Responsibilities:
Recruitment and Retention:
· Monitor recruitment/retention progress for the study, both weekly and overall.
· Coordinate with NP interventionist to help facilitate logistics for providing the intervention to participants. Ensuring appropriate participant information is relayed in a timely manner, as well as assisting with intervention set-up as needed.
· Provides back-up for CRA in regards to recruitment. Consenting participants, answering participant questions, reviewing eligibility requirements on a case-by-case basis and assisting with participant lab draws as needed.
Laboratory Management:
· Maintains sample integrity in the on-site laboratory. Monitoring temperatures, managing freezer maintenance, and organizing and documenting samples for easy access.
· Monitoring laboratory supply levels and working with PI to reorder as needed.
· Coordination with consulting laboratory regarding ELISA testing. This includes monitoring samples, communicating with their lab technician in regards to ELISA timing, and transporting samples to the lab site.
· Coordinating with the statistician and PI in regards to group allocation during monthly randomization.
Coordinating Aspects of Care:
· Coordination with CRA in regards to participant appointments.
· Coordinating with PI in regards to monitoring for adverse events and participant depression scores, responding to high scores as indicated per protocol.
· Potential for monitoring data entry by Clinical Team Member (CTMB), assuring data is entered completely and accurately.
Administrative:
· Assists CRA as needed to maintain study records and ensures compliance with HIPAA.
· Assists PI with study-related paperwork as needed.
Position Preferences/Requirements:
· Ideally, candidate will have a bachelor’s degree in nursing.
· Experience with clinical trial research, especially biological and behavioral research.
· Previous clinical experience in NICU, Labor & Delivery or Mother/Baby is preferred.
· Phlebotomy skills are required.
· Candidate must be able to work with an interdisciplinary team, have good organizational skills, excellent communication skills and be flexible.
Company DescriptionSmall company with history of established science with NIH- funded research in the maternal/fetal medicine realm.Company DescriptionSmall company with history of established science with NIH- funded research in the maternal/fetal medicine realm.-
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