Remote Hematopoietic Research Coordinator

Fred Hutch

Seattle (WA)

Hybrid

USD 37,000 - 52,000

Full time

2 days ago
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Job summary

Fred Hutchinson Cancer Center in Seattle seeks a Clinical Research Coordinator I to organize and manage day-to-day operations of hematopoietic cell transplantation observational studies. You will screen patients, coordinate visits, and ensure data quality per IRB protocols.

Work may be performed on-site with partial remote capabilities; strong regulatory knowledge and data management skills are essential for success in this role.

Qualifications

  • Minimum one year of experience in a clinical research or cancer registry environment with regulatory or human research protections.
  • Ability to apply judgement in interpreting regulations, determining impacts, and knowing when to elevate questions and concerns when appropriate.

Responsibilities

  • Serve as designee of the Principal Investigator (PI) to manage the daily clinical operations of assigned research studies in accordance with regulatory, GCP guidelines and institutional policy.
  • Assist the Principal Investigator (PI) with scheduling and taking minutes during conference calls and creating reports.
  • Abstract charts to collect study data and enter data into study databases.
  • Develop and maintain tools for study implementation, which may include data collection tools and study reference materials.
  • Initiate scheduling of patient clinic visits and ongoing study visits, ensuring procedures and tests are completed as outlined in protocols.
  • Complete requisition forms, assemble kits, transport laboratory samples, and maintain study supplies.

Skills

Clinical research
Regulatory knowledge
Attention to detail

Education

High school diploma or equivalent

Job description

Fred Hutchinson Cancer Center in Seattle seeks a Clinical Research Coordinator I to organize and manage day-to-day operations of hematopoietic cell transplantation observational studies. You will screen patients, coordinate visits, and ensure data quality per IRB protocols.

Work may be performed on-site with partial remote capabilities; strong regulatory knowledge and data management skills are essential for success in this role.

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