Clinical Research CoordinatorApply Now
Location: , Idaho
Employment Type: Contract
Job Description
Contract Length: 6 months with possible extension, onsite position
Responsibilities:
Requirements:
Responsibilities:
- Continues to display a mastery of Senior Clinical Research Associate duties and responsibilities
- Adheres to Standard Operating Procedures (SOP), GCP, all regulatory practices as established by law, and company policies and procedures
- Develops in-depth understanding of each study protocol to ensure all aspects of the protocol are adhered to in accordance with Food and Drug Administration (FDA), GCP, and ICH Guidelines
- In collaboration with the PI, incorporates knowledge of protocol to identify potential study participants according to inclusion/exclusion criteria
- Develops processes for monitoring the status of study subjects as they progress through the study protocol assessment timeline
Requirements:
- Bachelor’s Degree or an equivalent combination of education and experience
- 2+ years’ healthcare experience with Renal experience preferred; research experience preferred
- Willing to pursue CCRC or SoCRA certification when eligible
- Current appropriate state licensure if applicable
- Proficient with PCs and Microsoft Office applications
- Good communication and organizational skills
- Ability to work independently
Contact
Derek Crowley
Technical Recruiter
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