Onsite Clinical Research Coordinator: Patient Care

IQVIA; Parsippany-Troy Hills (NJ); 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 clinical procedures, recruit and screen patients, and ensure adherence to study protocols and GCP guidelines.

Responsibilities include coordinating studies, maintaining data integrity in CRFs/EDC, and supporting investigators and monitors to deliver high-quality results while prioritizing patient safety and compliance.

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 ECGs, sample collection, and vital signs assessments.
• Coordinate clinical research studies and maintain compliance with study protocols and GCP guidelines.
• Conduct patient study visits and support participants throughout the research process.
• Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient patients, evaluating eligibility based on criteria while ensuring safety.
• Collect, enter, and maintain accurate clinical data in CRFs and EDC systems.
• Assist with EDC query management and resolution, ensuring data accuracy and quality.
• Collaborate with investigators, sponsors, and monitors to address study-related issues.
• Act as a patient advocate and maintain a safe environment per Health and Safety policies.

Skills

Clinical research experience

GCP knowledge

Patient visits

EDC proficiency

Data integrity

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 clinical procedures, recruit and screen patients, and ensure adherence to study protocols and GCP guidelines.

Responsibilities include coordinating studies, maintaining data integrity in CRFs/EDC, and supporting investigators and monitors to deliver high-quality results while prioritizing patient safety and compliance.