Clinical Research Nurse

University Cancer & Blood CenterAthens, GA
1d

About The Position

The Clinical Research Nurse/Coordinator supports, coordinates, and leads clinical research studies—ranging from industry-sponsored trials to government-funded and investigator-initiated projects. This role ensures efficient progress from planning and approval through study closure, including participant recruitment, data collection, regulatory compliance, and billing coordination.

Requirements

  • Registered Nurse (RN) license
  • Excellent organizational, communication, and coordination ability across multidisciplinary teams.
  • Proficiency in Computer skills such as Microsoft Office suite.

Nice To Haves

  • Advanced certification (CCRC, CCRP) or Prior Clinical Research experience advantageous.

Responsibilities

  • Collaborate with the Principal Investigator (PI) to ensure adherence to study protocols and regulatory requirements.
  • Screen, recruit, and enroll participants; explain protocols and secure informed consent.
  • Schedule and conduct patient visits: perform assessments, vitals, ECGs, labs, administer investigational treatments, and monitor for adverse events (AEs/SAEs).
  • Document and enter clinical findings into source documents, CRFs/eCRFs, and sponsor databases accurately and on time.
  • Extract, collect, and manage study-related data from medical records and other sources.
  • Maintain accurate, up-to-date regulatory binders and documentation, including informed consent forms, IRB submissions, and study logs.
  • Ensure compliance with GCP, FDA, OHRP, and institutional guidelines.
  • Document and report all AEs and SAEs per protocol, sponsor, and regulatory timelines.
  • Oversee investigational product ordering, receipts, storage, preparation, and accountability logs.
  • Coordinate laboratory specimen collection, labeling, processing, and shipment per protocol.
  • Contribute to protocol development, site feasibility assessments, budgeting, and study start-up tasks.
  • Assist with staff training, onboarding, and continuous process improvement.
  • Participate in monitoring visits, audits, and sponsor/CRO oversight activities.
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service