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Clinical Research Coordinator

1 week ago


Baltimore, Maryland, United States Johns Hopkins University Full time

**Job Summary**

We are seeking a highly skilled Clinical Research Coordinator to facilitate clinical research patient visits and data collection at the James Brady Urological Institute at Johns Hopkins University. This position will support clinical trials, including attending clinical trial biopsy procedures, collection, handling, and transport of patient specimens to ensure quality samples, assisting with data collection and clarification, and general administrative duties.

The ideal candidate will have a strong background in medical or laboratory research and excellent communication and interpersonal skills. They will work closely with faculty and staff, including PIs, research nurses, study coordinators, and Sr. Clinical Research Program Manager.

  • Responsibilities:
  • Attend clinical trial required biopsy procedures, collect, handle, and transport patient samples.
  • Act as department liaison with outside support groups, including multiple research laboratories both in-house and third-party.
  • Anticipate daily changes in schedule, maintaining a smooth patient flow.
  • Use universal safety precautions to protect self and co-workers from biohazardous materials, including blood-borne pathogens.
  • Learns and follows all study procedures and protocols.
  • Assist clinical research staff with data collection, including obtaining medical records, lab results, diagnostic results, visit notes, data entry, and data clarification.
  • Assist nursing staff to prepare for research patient visits, help with research kit preparation and inventory, and meal and parking vouchers.
  • Assist study coordinator staff with ordering archival tissue from internal and external sources.
  • Participate in routine group meetings and/or study-specific teleconference.
  • Perform general administrative tasks, including copying, faxing, maintaining office supplies, and errand running.
  • Assist with study invoicing and reimbursement requests.
  • Comply with Good Clinical Practices, ICH Guidelines, and Clinical Research Office policies.

Requirements

  • High School Diploma or graduation equivalent.
  • Two years related experience.
  • Addition education may substitute for required experience, to the extent permitted by the JHU equivalency formula.

This position requires a detail-oriented individual with excellent time management skills and the ability to manage multiple projects at once. The successful candidate will have outstanding organizational skills and the ability to prioritize tasks effectively.