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Laboratory Administrator - Clinical Sample Management & Blood Donor Program

Job in Orlando, Orange County, Florida, 32885, USA
Listing for: Yoh Services LLC
Full Time position
Listed on 2026-02-23
Job specializations:
  • Healthcare
    Clinical Research, Medical Science, Medical Technologist & Lab Technician
Salary/Wage Range or Industry Benchmark: 21 - 30 USD Hourly USD 21.00 30.00 HOUR
Job Description & How to Apply Below

Laboratory Administrator – Clinical Sample Management & Blood Donor Program

Location: Orlando, FL

Job Family: R&D Operations |
Job Profile: Laboratory Operations Support

About the Role

We are seeking a highly organized and detail-oriented Laboratory Administrator to join our Orlando R&D team. In this pivotal role, you will serve as the operational backbone for clinical Human Biological Sample (HBS) management and our Blood Donor Program, ensuring seamless sample lifecycle management from receipt through analysis and destruction. You will work at the intersection of clinical research operations and laboratory science, directly supporting the generation of critical biomarker and immunology data that advances our pipeline.

This role offers the opportunity to contribute to cutting‑edge research while maintaining the highest standards of quality, compliance, and scientific integrity.

Key Responsibilities Clinical Sample Management (60%) Sample Lifecycle Coordination
  • Lead end‑to‑end coordination of clinical HBS activities including receiving, verification, discrepancy resolution, logging, review, and distribution/shipping
  • Serve as the primary point of contact and subject matter expert for Orlando Sample Management documentation and binding processes
  • Manage clinical HBS inventory, storage conditions, and sample destruction in compliance with regulatory requirements and Sanofi quality standards
  • Coordinate backup staff coverage and cross‑train team members to ensure operational continuity
Clinical Documentation & Reporting
  • Author and review critical clinical documentation including:
    • Analytical Test Plans (ATPs) – approximately five reviews per cycle
    • Sample sections for Analytical Test Reports (ATRs) – approximately five per cycle
    • Sample Destruction Memos – approximately five per cycle
  • Ensure documentation accuracy, completeness, and compliance with GCP/GLP requirements
  • Support audit and inspection readiness by maintaining organized, accessible records
Blood Donor Program Administration (40%) Program Operations & Database Management
  • Administer project workflows in the Blood Database, including unit hold/reserve status management and researcher project permissions
  • Assign internal identifiers to blood units using established database protocols
  • Serve as primary contact for Benchling Biosource laboratory research needs
Logistics & Stakeholder Coordination
  • Coordinate with courier services for scheduling and transport of blood products
  • Interface with Orlando and off‑site colleagues to fulfill project‑specific donation requests
  • Organize domestic and international biospecimen shipments, including preparation of all required import/export documentation
Training & Technical Support
  • Lead training programs for blood processing activities and associated SOPs, maintaining active technical competency through regular hands‑on processing (minimum two‑four units monthly) to ensure training quality and procedural currency
  • Provide backup support for blood processing technicians during peak periods or absences
  • Contribute to continuous improvement of blood processing workflows and documentation
What You’ll Bring Education
  • Required: Bachelor’s degree in Biological Sciences, Biomedical Sciences, or related field
  • Preferred: Master’s degree in a relevant discipline
Experience
  • Required:
    • 3+ years of experience in laboratory operations, sample management, or R&D support within the pharmaceutical, biotechnology, or clinical research industry
    • Hands‑on experience with primary human biological samples, including processing, cryopreservation, and thawing of human PBMCs
    • Demonstrated experience with clinical study protocols and sample management requirements
    • Track record of managing documentation processes for human blood products
  • Preferred:
    • Experience with domestic and international biospecimen shipping regulations (IATA, DOT)
    • Familiarity with laboratory information management systems (LIMS) and biobanking databases
    • Prior experience in a GCP/GLP‑regulated environment
Technical Skills
  • Proficiency in sample tracking databases and laboratory information systems
  • Strong understanding of cold chain management and sample integrity requirements
  • Knowledge of regulatory requirements for…
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