Clinical Research Coordinator - Novi, MI

IQVIA•Parsippany, MI
•Onsite

About The Position

IQVIA is seeking a Clinical Research Coordinator to support clinical research studies under the supervision of a principal investigator. The on-site position is based in Novi, Michigan and is scheduled for 24 hours per week. It includes hands-on clinical procedures, community outreach, and responsibility for high standards of patient care and regulatory compliance. The coordinator conducts clinical procedures, coordinates study activities, recruits and supports patients, and collects and records study data. The role also involves preparing materials and equipment, collaborating with investigators and monitors, and maintaining a safe environment. The position is not eligible for sponsorship.

Requirements

  • At least 1 year of relevant work experience in clinical research.
  • Working knowledge of clinical trials, GCP principles, and medical terminology.
  • Experience prescreening patients based on inclusionary and exclusionary criteria.
  • Familiarity with reviewing patient charts and medical records.
  • Ability to support patient study visits.
  • Strong attention to detail and ability to establish effective working relationships.
  • Proficiency with EDC systems, accurate data entry, and query management.

Nice To Haves

  • Bachelor’s degree preferred, or an equivalent combination of education and relevant experience.

Responsibilities

  • Perform clinical procedures, including ECGs, sample collection, and vital signs.
  • Coordinate clinical research studies and maintain compliance with study protocols and Good Clinical Practice (GCP) guidelines.
  • Prepare study materials, set up equipment, and plan logistical activities to support study conduct.
  • Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
  • Collect and accurately record clinical data in case report forms (CRFs).
  • Collaborate with investigators and monitors, address queries, and ensure data quality.
  • Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.
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