Clinical Research Coordinator — On-Site, Patient-Centric Trials

IQVIA; Southfield (MI); On-site; USD 48,000 - 58,000; Full time

Job summary

IQVIA is seeking a Clinical Research Coordinator to join our on-site team in Southfield, MI. You will perform hands-on clinical procedures, coordinate studies, recruit and screen participants, and ensure adherence to GCP and study protocols.

This role supports patient visits, data capture, and data integrity, under supervision of a principal investigator. The ideal candidate has a bachelor's degree (or equivalent) with at least 1 year of clinical research experience, strong knowledge of GCP, and

Qualifications

• Bachelor's degree preferred or equivalent combination of education and relevant experience.
• Minimum 1+ years of relevant work experience in clinical research.
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Experience conducting patient study visits and participant-facing clinical research activities.
• Demonstrated ability to recruit and screen patients according to study eligibility criteria.
• Proficiency with EDC systems, including accurate data entry, query resolution, and data management processes.
• Strong attention to detail and ability to establish effective working relationships.

Responsibilities

• Perform a variety of clinical procedures, including ECGs, sample collection, and vital signs assessments.
• Coordinate clinical research studies and maintain compliance with study protocols and Good Clinical Practice (GCP) guidelines.
• Conduct patient study visits and support participants throughout the research process, ensuring a positive study experience.
• Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient patients, evaluating eligibility based on study inclusion and exclusion criteria while ensuring their safety and well‑being throughout the study.
• Collect, enter, and maintain accurate clinical data in case report forms (CRFs) and Electronic Data Capture (EDC) systems.
• Assist with EDC query management and resolution, working closely with investigators and monitors to ensure data accuracy, completeness, and quality.
• Collaborate with investigators, sponsors, and study monitors to address study-related issues and maintain high standards of data integrity.
• Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Skills

Clinical research

GCP knowledge

Data entry

Patient recruitment

EDC systems

Education

Bachelor's degree or equivalent

Tools

EDC software

Job description

IQVIA is seeking a Clinical Research Coordinator to join our on-site team in Southfield, MI. You will perform hands-on clinical procedures, coordinate studies, recruit and screen participants, and ensure adherence to GCP and study protocols.

This role supports patient visits, data capture, and data integrity, under supervision of a principal investigator. The ideal candidate has a bachelor's degree (or equivalent) with at least 1 year of clinical research experience, strong knowledge of GCP, and