Neurology Clinical Research Coordinator - Onsite

Indiana University Health; Fort Wayne (IN); On-site; USD 52,000 - 72,000; Full time

Job summary

Indiana University Health is seeking individuals who embody our values to join our Neurology Research team as Clinical Research Coordinator. This full-time, onsite role works Monday–Friday, 8:00am–4:30pm in our Fort Wayne offices, supporting groundbreaking clinical trials.

You will collaborate with patients, physicians and study teams, applying hands-on clinical skills with research coordination responsibilities, data management, regulatory compliance, and patient vitals.

Qualifications

• Bachelor's degree in life sciences or related field required or equivalent experience.
• Requires ability to obtain and apply knowledge of research operations.
• 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

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.

Skills

Microsoft Office proficiency

Clinical research coordination

Education

Bachelor's degree in life sciences or related field

Job description

Indiana University Health is seeking individuals who embody our values to join our Neurology Research team as Clinical Research Coordinator. This full-time, onsite role works Monday–Friday, 8:00am–4:30pm in our Fort Wayne offices, supporting groundbreaking clinical trials.

You will collaborate with patients, physicians and study teams, applying hands-on clinical skills with research coordination responsibilities, data management, regulatory compliance, and patient vitals.