Associate Clinical Research Coordinator - Part Time Evenings

About the role

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: Marsh Melvin Laird. Location: Marshfield, WI. Address: 701 W Kalsched St, Marshfield, WI 54449, USA. Shift: Evening. Job Schedule: Part time. Weekly Hours: 20.00. Salary Range: $20.50 - $33.00. In this on-site position in Marshfield, Wisconsin you'll gain hands-on experience in clinical research while supporting important cancer prevention and epidemiologic studies. This customer-focused role requires the ability to work independently while educating patients and collaborating with clinical staff throughout the research process.

Responsibilities

• Coordinating various aspects of clinical trials, including participant recruitment calls, screening and interviewing, scheduling study visits, and facilitating biospecimen collection.
• Assist and organize components of various clinical trials, including the coordination of study-required procedures, as well as investigational treatment for a variety of conditions and symptoms.
• Participate with direction in listing and clarifying questions and concerns with the investigator and sponsor regarding enrollment goals, sponsor expectations and study procedures.
• Assist with scheduling and coordinating 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 and data entry.
• Conduct interviews to assess subject ability and willingness to follow and complete study procedures and visits.
• Follow randomization procedures per protocol.
• Schedule subjects for follow-up 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