Clinical Research Coordinator - On Site Only
About The Position
Join the dynamic team at Great Plains Health and be a part of something truly exceptional. At Great Plains Health, we embody a culture defined by authenticity, integrity, and a genuine commitment to listening to both our patients and each other. As a member of our team, you'll experience a supportive environment where collaboration is key, and every voice is valued. We work together seamlessly, leveraging our collective strengths to provide the highest quality care to our community. Passion drives us forward, propelling us to constantly strive for excellence in everything we do. If you're seeking a rewarding career in healthcare surrounded by like-minded individuals who share your dedication and enthusiasm, Great Plains Health is the place for you. Come join us and be part of a team that's making a real difference every day.
Requirements
- Associates degree from a two year college or technical school (nursing, pharmaceutical or science related field) and six months experience in related medical fields preferred OR A general Associates degree and 1 year of direct responsibility for clinical research or one year as an Assistant Research Coordinator (ARC)
Nice To Haves
- State Required: None
- GPRMC Preferred: None
Responsibilities
- Develops basic knowledge of Good Clinical Practice guidelines, FDA guidelines, study protocols and informed consent process as they pertain to clinical research.
- Develops full knowledge of inclusion/exclusion for patient enrollment for all trials.
- Prepares all pertinent supplies, forms, etc., to expedite patient enrollment for all trials.
- Obtains training to appropriately collect and process blood and urine specimens for shipment to reference laboratories.
- Conducts the trial by working with patients, family and other health care providers by scheduling appointments for screening, medication administration and follow up visits for all trials.
- Submits data and information, and undertakes all assigned activities, so that the time schedules set forth in the protocol are strictly met.
- Completes, reviews, and maintains trial subject source documents.
- Interacts professionally with study sponsors and investigators while maintaining clinical research associated supplies, forms and inventory control of investigational agents in conjunction with the investigator.
- Provides assistance to visiting study monitors by producing appropriate documentation.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
