Clin Trials Rsrch Associate - ICTS Coordinator Core

University of Iowa • Iowa City, IA

7d • Hybrid

About The Position

Under the supervision of a physician, and/or Nurse Manager and/or designee, the clinical trial research associate will be an integral member of the research team in the Institute for Clinical and Translational Science. This position will provide support for the Institute for Clinical and Translational Science by performing activities which are vitally important to establish the research core for the department, as well as to grow and foster innovation through research support endeavors. The clinical trial research assistant will apply clinical skills to administer, deliver, and evaluate research protocols.

Requirements

• A Bachelor’s degree in a Health Science field or an equivalent combination of education and research experience.
• Minimum of 1 year in a healthcare setting or 1 year of clinical research experience.
• Excellent written and verbal communication skills with patients/families, and interdisciplinary team members as demonstrated through written and verbal interactions.
• Ability to work flexible hours including nights, evenings, and weekends as needed by the research protocol.
• Proficiency in Microsoft Word, Outlook and Excel.

Nice To Haves

• Basic clinical research experience.
• Working knowledge of Good Clinical Practice (GCP).
• Previous experience writing manuscripts for publication.
• Experience with REDCap, Epic, I-CART, and ACCESS.
• Previous experience in data collection and entry.
• Experience in processing research regulatory documents.
• A current license to practice nursing in Iowa by the time of hire.
• The ability to work independently.
• Excellent time management skills and ability to perform detail-oriented work.
• Current nursing licensure, or
• Current paramedic certification, or
• Current respiratory therapist certification or licensure.

Responsibilities

• Perform clinical/health care research activities in various departments.
• Screen, recruit, enroll and obtain informed consent for clinical research activities.
• Assist in the design, development, execution, administration and maintenance of protocols and clinical studies and provide input into descriptions of complex research procedures.
• Assist patients with problems related to protocol.
• Participate in the design, development, collection and testing of clinical research trial data systems.
• Acts as a liaison between health care clinical information systems and research data systems.
• Manage and organize regulatory documentation.
• Prepare and submit regulatory submissions.
• Participate in preparation of grant applications for extramural funding.
• Provide assistance with tracking and reconciling grant/trial budget free balances and identify opportunities to ensure that grant funding is being used as intended and awarded.

Benefits

• Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level