Clinical Research Coordinator - Neurology

Indiana University Health System • Fort Wayne, IN

2d • Onsite

About The Position

Indiana University Health is seeking individuals who embody excellence, compassion, teamwork, and purpose to join our Neurology Research team in the role of Clinical Research Coordinator. This position will work full time, onsite, Monday – Friday, 8:00am – 4:30pm in our Fort Wayne offices. In this role, you'll work closely with patients, physicians, and research teams throughout the study process, combining hands-on clinical skills with research coordination responsibilities. IU Health leaders play a crucial role in advancing the mission of our organization and inspiring teams to make a meaningful difference in the lives of patients. As one of Indiana’s largest employers and the most comprehensive medical system in the state, our vision is to lead the transformation of healthcare through quality, innovation and education, and make Indiana one of the nation’s healthiest states. IU Health, in partnership with the Indiana University School of Medicine, bring together highly skilled physicians, researchers, and educators into close collaboration to provide world-class care for children and adults and improve the health of patients and communities across Indiana.

Requirements

• Bachelor's degree in life sciences or related field required or equivalent experience.
• Requires ability to obtain and apply knowledge of research operations.
• Requires ability to obtain and apply knowledge of the organization policies and procedures.
• Requires proficiency in Microsoft Office and applications.
• Requires 0-3 years of relevant research data management experience.
• May require relevant certification specified by department leadership within 2 years of hire date

Nice To Haves

• 3-5 years preferred of relevant research data management experience
• A Clinical Background (Medical Assistant, Patient Care Assistant, RN, etc.).

Responsibilities

• Coordinates and provides overall project management support for the planning, initiation, monitoring, reporting, and completion of clinical research activities.
• Assists with the data management of clinical research programs and projects.
• Ensures industry quality standards for clinical activities are met and promotes continuous quality improvement.
• Assures compliance with protocols and conducts activities in accordance with regulatory requirements.
• Managing patient vitals, drawing labs, completing EKGs.

What This Job Offers

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