Lab & Biobanking Clinical Research Coordinator I

Meharry Medical College

Nashville (TN)

Vor Ort

USD 42.000 - 54.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Meharry Medical College is seeking a Clinical Research Coordinator I to manage specimen collection, processing, shipping, and tracking for the T4C initiative, while maintaining inventory and lab cleanliness in accordance with biosafety guidelines. The role involves coordinating IRB submissions, adhering to HIPAA, FDA, and GCP guidelines, and supporting budget and contracts under the PI.

Experience in clinical research, REDCap, EMR, LIMS is preferred, with a focus on regulatory compliance and

Qualifikationen

  • Graduated from an accredited discipline-specific program and licensed as phlebotomist/lab technician in Tennessee.
  • 5+ years experience in patient care or research setting preferred.
  • Bachelor’s degree in a healthcare-related field required; phlebotomist license preferred.

Aufgaben

  • Assess eligibility via screening interviews, medical record reviews, and clinician discussions.
  • Maintain case report forms, consent forms, and regulatory records.
  • Monitor budgets, invoices, and contracts under PI supervision.
  • Perform protocol procedures including venipuncture and vital signs.
  • Coordinate specimen collection, labeling, storage, and shipment.
  • Ensure study activities comply with protocols and regulations.

Kenntnisse

Clinical research knowledge
Regulatory compliance
IRB/GCP/HIPAA familiarity
Laboratory data entry
Teamwork
Vigilance under pressure

Ausbildung

Bachelor's degree in healthcare
Licensed phlebotomist (preferred)

Tools

REDCap
EMR
CTMS
LIMS

Jobbeschreibung

Meharry Medical College is seeking a Clinical Research Coordinator I to manage specimen collection, processing, shipping, and tracking for the T4C initiative, while maintaining inventory and lab cleanliness in accordance with biosafety guidelines. The role involves coordinating IRB submissions, adhering to HIPAA, FDA, and GCP guidelines, and supporting budget and contracts under the PI.

Experience in clinical research, REDCap, EMR, LIMS is preferred, with a focus on regulatory compliance and

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