Neurology Clinical Research Coordinator – Onsite, Full-Time

Myana

Fort Wayne (IN)

On-site

USD 55,000 - 75,000

Full time

11 days ago
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Job summary

Indiana University Health is seeking a Clinical Research Coordinator to join the Neurology Research team in Fort Wayne. This full‑time, on‑site role supports patient‑centric clinical trials, coordinating data, schedules, and regulatory compliance while collaborating with physicians and study staff.

The ideal candidate has a clinical background, data management skills, and the ability to navigate research operations and policies.

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 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.

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

Data management
Clinical background
Regulatory knowledge

Education

Bachelor's degree in life sciences or related field

Tools

Microsoft Office

Job description

Indiana University Health is seeking a Clinical Research Coordinator to join the Neurology Research team in Fort Wayne. This full‑time, on‑site role supports patient‑centric clinical trials, coordinating data, schedules, and regulatory compliance while collaborating with physicians and study staff.

The ideal candidate has a clinical background, data management skills, and the ability to navigate research operations and policies.

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