Clinical Research Coordinator

About this role

• **Careers With Purpose** **Sanford Health, the largest rural health system in the United States, is dedicated to transforming the health care experience and providing access to world-class health care in America's heartland.** **Facility:** Cancer Center Building **Location:** Sioux Falls, SD **Address:** 1309 W 17th St, Sioux Falls, SD 57104, USA **Shift:** 8 Hours - Day Shifts **Job Schedule:** Full time **Weekly Hours:** 40.00 **Salary Range:** $24.00 - $38.50 **Department Details** In this position you'll gain experience in clinical research and work with a variety of trials.
• This role requires educating patients, physicians, nurses, and other staff about the research process.
• It also involves organizing all aspects of clinical trials, including outreach, interviewing, scheduling, and coordinating tests and procedures A Bachelor's degree in biology, microbiology or related field is required.
• **Job Summary** Provides an opportunity to learn daily and contribute to treatments of the future.
• Enthusiasm for learning required, along with participation in educating patients, physicians, nurses and other personnel about the research process.
• Organize complex components of various clinical trials, including the coordination of study-required testing and procedures, as well as investigational treatment for a variety of conditions and symptoms.
• Participate in listing and clarifying questions and concerns with the investigator and sponsor regarding enrollment goals, sponsor expectations and study procedures.
• Schedule and coordinate pre-study site visits.
• Monitor enrollment goals and modify recruitment plan as necessary.
• Maintain patient screening/enrollment logs and appropriately update sponsors, contract research organizations (CROs) and/or senior medical officers (SMOs).
• Assure the completion of all screening, eligibility and enrollment procedures.
• Conduct interviews to assess subject ability and willingness to follow and complete study procedures and visits.
• Review diaries and questionnaires completed by subjects.
• Ensure appropriate specimen collection, batching and shipping as required.
• Collect source documents for sponsor or audit review.
• Assess subject compliance with the test article and follow-up visits.
• Abstract data from medical records, clinic, consultation and referral notes for preparation of study forms and flow sheets.
• Review inclusion/exclusion criteria to assure subject eligibility, and review with physician investigator for final sign-off.
• Review and verify required source documents in subject medical records to confirm study eligibility.

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