Clinical Research Coordinator - Southfield, MI

IQVIA•Parsippany, MI

5d•Onsite

About The Position

IQVIA is seeking a Clinical Research Coordinator (CRC) to support clinical research studies under the supervision of a principal investigator. The position involves conducting hands-on clinical procedures, coordinating study activities, engaging with the community, and maintaining high standards of participant care and regulatory compliance. The role is based on-site in Southfield, Michigan, and is scheduled for 40 hours per week. The CRC conducts participant visits and supports patients throughout the research process, including recruitment, screening, and orientation. The coordinator prepares study materials and equipment, collects and maintains clinical data, and works with investigators, sponsors, and study monitors to resolve study and data issues. The position also requires promoting participant safety and following study protocols, Good Clinical Practice guidelines, and Health and Safety policies. The potential base pay range is $35.00–$42.00 per hour. The actual offer may vary based on job-related qualifications, location, and schedule. Depending on the position offered, incentive plans, bonuses, and/or other compensation may be available, along with health and welfare benefits. 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 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.
Ability to establish effective working relationships.

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 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.
Prepare study materials, set up equipment, and plan logistical activities to support study conduct.
Recruit, screen, and orient patients; assess eligibility using study inclusion and exclusion criteria while protecting participant safety and well-being.
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 in collaboration with investigators and monitors.
Work with investigators, sponsors, and study monitors to address study-related issues and maintain data integrity.
Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.