Clinical Trials Operations & Specimen Coordinator

Yale Cancer Center

New Haven (CT)

On-site

USD 62,000 - 92,000

Full time

5 days ago
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Job summary

Yale Cancer Center is seeking an Operations Coordinator for the Clinical Research Support Laboratory (CRSL) within the Clinical Trials Office in New Haven. The role focuses on coordinating central research specimen requirements, logistics, and billing oversight across CTO studies.

You will collaborate with CRSL management to implement workflows, manage courier schedules, and maintain patient files while interfacing with Clinical Operations and study sponsors.

Qualifications

  • Bachelor’s? Actually the posting requires a Master’s degree in a scientific discipline and one year of experience.
  • Demonstrated knowledge of medical and laboratory terminology.
  • Excellent time management and organizational skills with multiple projects.

Responsibilities

  • Recommend the design and implementation of procedures and protocols under supervision.
  • Investigate and analyze research planning and results.
  • Ensure data results are compiled, analyzed, and presented properly.
  • Maintain clear documentation of results and prepare reports for proposals.
  • Perform independent research and participate in planning.
  • Interact with PI, staff, and external contacts to discuss results and ensure safe operation of the laboratory.
  • May perform other duties as assigned.

Skills

Interpersonal skills
Analytical thinking
Medical terminology
Time management
MS Office
OnCore
EPIC

Education

Master’s degree in a scientific discipline

Tools

OnCore
EPIC
MS Office

Job description

Yale Cancer Center is seeking an Operations Coordinator for the Clinical Research Support Laboratory (CRSL) within the Clinical Trials Office in New Haven. The role focuses on coordinating central research specimen requirements, logistics, and billing oversight across CTO studies.

You will collaborate with CRSL management to implement workflows, manage courier schedules, and maintain patient files while interfacing with Clinical Operations and study sponsors.

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