Clinical Trials Assistant

JOB SUMMARY

Perform a variety of duties include coordinating aspects of clinical trial protocols including but not limited to study initiation, recruitment, study visits, monitor visits, regulatory compliance, and study close-out.

ESSENTIAL DUTIES/RESPONSIBILITIES

• Act as a liaison between providers, study representatives and patients.
• Maintain case report forms, source documents and regulatory documents.
• Pack and ship patient labs and review lab results.
• Provide patient care and collect medical information during visit.
• Initiate and participate in the informed consent process.
• Conduct screening of prospective study participants and schedule appointments of patients interested in research studies.
• Instruct patients regarding study protocols.
• Arrange for or perform phlebotomy.
• Assist in formulating and actively participate in the subject recruiting process.
• Perform related work as required.

QUALIFICATIONS

• High School Diploma or equivalent.
• 2-5 years of experience in a clinical setting a plus.
• Phlebotomy experience/certification preferred.
• Certified Nurse Assistant Certificate and/or graduation from an accredited program for medical assistants a plus.
• Knowledge of Good Clinical Practices for clinical research a plus.
• Knowledge of OSHA and FDA regulations regarding clinical research a plus.
• Knowledge of medical terminology a plus.
• Knowledge of electronic medical record and scheduling system a plus.
• Experience in working with providers and other department staff.
• High level of computer competency.
• Ability to work independently, prioritize and work in a team environment.

This job description may not be inclusive of all assigned duties, responsibilities, or aspects of the job described, and may be amended at any time at the sole discretion of Hutchinson Clinic.