Biorepository Coordinator I PMI
About The Position
The Biorepository Staff Member is responsible for supporting the day-to-day operational functions of the biorepository, including the procurement of human biospecimens from surgical pathology, patient consent, specimen shipping, data entry, and quality assurance/quality control (QA/QC). Staff are expected to develop competency across all operational areas of the biorepository and will rotate through each area as experience and proficiency are established. As a result of this rotational model, scheduled work hours and shift assignments are subject to change in accordance with the operational needs of the biorepository and the area to which the staff member is currently assigned. Because each operational area functions under different collection and processing schedules — including early morning surgical start times, patient pre-operative consent windows, and shipping carrier pickup deadlines — scheduled hours and shift start/end times will vary accordingly. Candidates will initially be placed in the operational area most closely aligned with their prior experience and demonstrated competencies, with rotation into additional areas occurring as proficiency is established and operational needs require.
Requirements
- Bachelor of Science degree in a biological science, clinical laboratory science, or related field required
- Strong attention to detail, documentation accuracy, and the ability to work independently under defined protocols
- Effective interpersonal and communication skills required for patient-facing consent activities
Nice To Haves
- Prior experience in a clinical laboratory, pathology, or research setting preferred
- Familiarity with LIMS platforms, biospecimen handling, or clinical research operations preferred
Responsibilities
- Identify eligible patients from surgical schedules and coordinate consent activities in advance of scheduled procedures
- Present study information to patients and/or their authorized representatives in a clear, objective, and non-coercive manner
- Obtain and document informed consent in accordance with IRB requirements, institutional policies, and applicable federal regulations
- Maintain accurate and auditable consent records within the LIMS and/or institutional document management system
- Perform accurate and timely data entry of specimen collection, processing, storage, and transfer records into the LIMS
- Conduct routine QA/QC audits of specimen records, including reconciliation of physical inventory against LIMS data and identification of documentation discrepancies
- Flag and escalate data integrity issues, SOP deviations, or specimen quality concerns to the Biorepository Manager in accordance with established reporting procedures
- Support the preparation of QA/QC reports, audit documentation, and regulatory compliance records as directed
- Prepare specimens for shipment in accordance with IATA Packing Instruction biological substances (Category B) and applicable IATA Dangerous Goods Regulations
- Verify chain-of-custody documentation and ensure accurate specimen labeling with 2D barcode or linear barcode identifiers prior to shipment
- Coordinate with receiving institutions to confirm shipping requirements, confirm receipt, and document chain-of-custody transfer in the LIMS
- Maintain shipping logs and investigate and document any temperature excursions, shipping delays, or specimen integrity concerns
Benefits
- health
- disability
- retirement
- wellness offerings
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
