Clinical Research Coordinator, Biospecimen Management

2 months ago

Bethesda, United States Kelly Full time

he National Institutes of Health is seeking a Clinical Research Coordinator. This is a long-term, full-time, contract position based in Bethesda, MD. This is an on-site position. This position offers a competitive benefits package.


Position Summary:

The Translational Immunopsychiatry Unit (TIU) is seeking an ambitious, conscientious, organized, and detail-oriented Clinical Research Coordinator (CRC) with strong interpersonal and communication skills to join our growing team at the National Institutes of Health (NIH). This CRC

position will be supporting the National Institute of Mental Health (NIMH), located in Bethesda, MD. The primary responsibilities for this full-time on-site CRC position will be to provide clinical and biospecimen research coordination for the TIU and affiliated programs, including the Autoimmune Brain Disorders Program (ABDP).


PRIMARY RESPONSIBILITIES:

  • Update biospecimen management systems data systems SOPs as needed in the TIU Handbook
  • Support the unit with one (1), active IRB protocol, a secondary use protocol for biomarker discovery in blood and CSF. The TIU has one (1) secondary use remote biospecimen collection protocol that is under scientific review. This protocol will allow for the enrollment of surplus biospecimens that are no longer needed for clinical testing.
  • Supervise post-bac IRTAs responsible for biospecimen pick-up and transport.
  • Establish SOPs for biospecimen transport and supervise post-bac IRTAs, who will be responsible for physically transporting the biospecimen.
  • Ensures that biospecimen management SOPs are consistent with CLIA requirements.
  • Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.
  • Implement the existing method for transferring data from the NIH medical record system BTRIS into BRICS.
  • Work with instituional supportImplement system for uploading outside clinical records, outside diagnostic tests, interviews, and questionnaires/surveys to research subject entries in BRICS.
  • Prepares reports – On a semiannual basis, prepare reports that provide an overview of biospecimen program
  • Develops and implements systems for importing clinical data into the Biomedical Research Informatics Computing System (BRICS):
  • Assist with subject enrollment, scheduling outpatient appointments and inpatient admissions, travel arrangements, consent, and assent.
  • Instruct data entry and clinical staff in procedures relative to data management, protocol instructions, Standard Operating Procedures and regulatory processes and considerations.
  • Prepare materials, coordinate scheduling, track attendance and report results of workshops related research best practices, emerging trends in clinical studies, new literature and findings and regulatory considerations.


REQUIREMENTS:

  • Master's degree in Biology, or related discipline.
  • Minimum 5 years of clinical research experience is required
  • Experience developing Standard Operating Procedures is required
  • Experience in maintaining clinical research databases is preferred

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