Clinical Research Coordinator I - Temporary
About The Position
The Clinical Research Coordinator helps to organize and carry out day-to-day operations and administrative functions of investigator-initiated and industry-sponsored human subjects clinical trials. This individual will work under general supervision of the Principal Investigator, Clinical Research Nurse or Clinical Research Manager and will be required to perform his/her responsibilities with limited degree of independence within the scope of study protocol(s) and institutional policies and guidelines. At Fred Hutchinson Cancer Center, all employees are expected to demonstrate a commitment to our values of collaboration, compassion, determination, excellence, innovation, integrity, and respect.
Requirements
- 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.
Nice To Haves
- Associate or bachelor’s degree preferred.
- Certified Clinical Research Coordinator (CCRC) or certification as Clinical Research Professional (SOCRA).
- Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
- Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
- Two years of experience in a research environment with regulatory or human research protections.
- Previous experience working with NIH, FDA and OHRP regulations and medical terminology.
- Knowledge of clinical trials records, procedures, and computerized data processing systems.
- Ability to extract data from medical records.
Responsibilities
- Helps to organize and carry out day-to-day operations and administrative functions of investigator-initiated and industry-sponsored human subjects clinical trials.
- Will work under general supervision of the Principal Investigator, Clinical Research Nurse or Clinical Research Manager
- Will be required to perform his/her responsibilities with limited degree of independence within the scope of study protocol(s) and institutional policies and guidelines.
Benefits
- retirement savings plan
- employee assistance program
- paid sick leave (1 hour for every 30 hours worked)
- prorated paid holidays (up to 11 days per year)
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
