Clinical Research Coordinator I - Myeloma
Fred Hutchinson Cancer Center
- Pay
- $27 to $39
- an hour
- Location
- Seattle, WA
- Job type
- Full time
- Posted
- Nov 7
- 1 day ago
Career path
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About the company
Fred Hutchinson Cancer Center
Fred Hutchinson Cancer Center is an independent, nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. Based in Seattle, Fred Hutch is the only National Cancer Institute-designated cancer center in Washington. With a track record of global leadership in bone marrow transplantation, HIV/AIDS prevention, immunotherapy and COVID-19 vaccines, Fred Hutch has earned a reputation as one of the world’s leading cancer, infectious disease and biomedical research centers. Fred Hutch operates eight clinical care sites that provide medical oncology, infusion, radiation, proton therapy and related services, and network affiliations with hospitals in five states. Together, our fully integrated research and clinical care teams seek to discover new cures to the world’s deadliest diseases and make life beyond cancer a reality.
What you'll do
- Manage daily clinical operations of assigned research studies
- Review study candidates’ medical records for study eligibility
- Arrange consent meetings with potential patients and participate in consenting as permitted
- Arrange ordering and scheduling of sample collection and coordinate transport to Fred Hutch labs
- Develop and maintain tools for tracking participants during treatment and beyond
- Function as a protocol liaison with clinical teams, patients, and others
- Provide input regarding IRB correspondence and regulatory documentation
- Extract targeted data from medical records based on clinical protocol
What you need
- High school diploma or equivalent.
- Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.
- Demonstrated knowledge of how to synthesis study conduct.
- Ability to apply judgement in interpreting regulations, determining impacts, and knowing when to escalate questions and concerns when appropriate.
- Associate's degree or higher in related area
- Minimum of 1-2 years experience in a clinical research setting
- Certified Clinical Research Coordinator (CCRC) or certification as Clinical Research Professional (SOCRA)
- Must have excellent communication and organizational skills
- Experience with Microsoft Office (Excel, Access, Word)
- Must be a self-starter with the ability to locate resources and operate productively in an environment where standard operating procedures, guidelines and policies are not always available
- This position requires excellent organizational skills, attention to detail, and ability to problem solve
- Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills
- Must have the flexibility to manage patients visits that may occur before or after regular work hours
- Knowledge of clinical trials records, procedures, and computerized data processing systems.
- Ability to extract data from medical records.
- Education: a high school diploma or an associate degree
Key skills
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Perks
- medical/vision
- dental
- flexible spending accounts
- life
- disability
- retirement
- tuition reimbursement
- paid vacation
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