Biobank Operations Specialist: Clinical Research

The Nemours Foundation; Wilmington (DE); On-site; USD 55,000 - 75,000; Full time

Job summary

The Nemours Foundation seeks a Clinical Research Technologist I to support the Lung Health Cohort biobank operation in Wilmington, DE. This role manages receipt, storage, and shipment of biospecimens and prepares regulatory reports under NIH-funded protocols.

The position involves maintaining both handwritten and computerized specimen records, coordinating material transfer agreements, and contributing to SOP development with BMAP leadership and investigators.

Qualifications

• Bachelor's degree or MT with equivalent experience.
• Knowledge of QC and QA as applied to clinical diagnostic testing.
• Experience with clinical lab procedures required of a CAP and/or CLIA certified laboratory.
• 1-3 years experience

Responsibilities

• Receives biospecimens from the LHC collection sites into the ALA-ACRC biorepository housed at Nemours Biobank and Molecular Analysis Program (BMAP), tracking incoming shipments and cataloguing biospecimens.
• Prepares biospecimens for shipment to investigators under approved protocols, tracks shipments, and completes related paperwork and data entry.
• Prepares reports of biospecimens received and shipped as requested.
• Assists with budgets, material transfer agreements, and other regulatory documents; coordinates shared email baskets.
• Develops SOPs with BMAP leadership and investigators; coordinates order placement for supplies.
• Maintains custody and tracking of biospecimens per SOPs and regulatory guidelines

Skills

QC/QA knowledge

Clinical lab experience

Education

Bachelor's degree or MT with equivalent experience

Job description

The Nemours Foundation seeks a Clinical Research Technologist I to support the Lung Health Cohort biobank operation in Wilmington, DE. This role manages receipt, storage, and shipment of biospecimens and prepares regulatory reports under NIH-funded protocols.

The position involves maintaining both handwritten and computerized specimen records, coordinating material transfer agreements, and contributing to SOP development with BMAP leadership and investigators.