Manager of Tissue Operations

Sarah Cannon Research InstituteNashville, TN

About The Position

As the Manager of Tissue Operations you will provide operational and people leadership for Tissue Operations to ensure timely, high-quality procurement, processing, and management of tissue samples supporting clinical research activities. This role is accountable for end-to-end workflow oversight, turnaround time (TAT) performance, cross-functional coordination, and continuous process improvement. The Manager ensures consistent execution of tissue operations, establishes clear accountability for prioritization and escalation, and develops staff to support a scalable, high-performing function.

Requirements

  • Clinical research operations, including tissue and specimen management workflows
  • Regulatory, sponsor, and quality requirements related to specimen handling
  • Process improvement and performance metric tracking
  • Operational leadership and team management
  • Process design, workflow optimization, and problem-solving
  • Data analysis and performance tracking
  • At least three years of experience in clinical research, laboratory operations, or tissue/specimen management.

Responsibilities

  • Oversees end-to-end tissue operations, including procurement, receipt, processing, documentation, shipment, and return of fresh and archival specimens
  • Directly manages Tissue Operations staff, including hiring, onboarding, performance management, and professional development
  • Establishes clear expectations, accountability, and workload prioritization across the team
  • Ensures appropriate coverage, workload distribution, and operational readiness
  • Owns tissue turnaround time (TAT) performance, including prioritization decisions and intervention strategies
  • Tracks, trends, and analyzes key metrics (e.g., fresh, archival, priority TAT) to drive performance improvement
  • Drives accountability for meeting defined operational targets and service-level expectations
  • Ensures compliance with SOPs, work instructions, sponsor requirements, and regulatory standards
  • Develops, implements, and maintains SOPs and work instructions to support consistent operations
  • Ensures adherence to corporate policies, quality standards, and audit readiness expectations
  • Identifies process gaps and implements sustainable workflow improvements to enhance efficiency and reduce delays
  • Partners with internal teams (physicians, research nurses, coordinators, laboratory staff) to ensure alignment on study needs and timelines
  • Coordinates with external partners (pathology labs, sponsors, CROs) to support timely specimen procurement and issue resolution
  • Serves as escalation point for complex or time-sensitive issues impacting specimen flow or study timelines and addresses concerns as needed with leadership and physicians
  • Ensures consistent, high-quality communication and service across internal and external stakeholders
  • Supports training, competency development, and ongoing education for the team

Benefits

  • Comprehensive benefits to support physical, mental, and financial well-being
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