On-Site Part-Time Clinical Research Coordinator – Elevate Trials

IQVIA Inc; Novi (MI); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA is seeking a Clinical Research Coordinator to join our Novi, MI team on-site. This 24-hour/week role involves hands-on procedures, subject recruitment, data collection, and ensuring study conduct adheres to GCP and protocol requirements.

Under supervision of a principal investigator, you will perform ECGs, vital signs, and sample collection, maintain study documents, and support logistics for ongoing trials. Bachelor’s degree preferred with 1+ year of clinical research experience.

Qualifications

• Bachelor’s degree or equivalent in a relevant field.
• Minimum 1+ year of clinical research experience.
• Familiarity with GCP, medical terminology, and patient safety.

Responsibilities

• Perform ECGs, sample collection, and vital signs.
• Coordinate studies and ensure GCP compliance.
• Prepare materials, set up equipment, plan logistics.
• Recruit, screen, and orient patients.
• Record data in CRFs with accuracy.
• Collaborate with investigators and monitors.

Skills

Prescreening experience

EDC systems proficiency

Clinical data management

Attention to detail

Education

Bachelor’s degree or equivalent

Tools

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator to join our Novi, MI team on-site. This 24-hour/week role involves hands-on procedures, subject recruitment, data collection, and ensuring study conduct adheres to GCP and protocol requirements.

Under supervision of a principal investigator, you will perform ECGs, vital signs, and sample collection, maintain study documents, and support logistics for ongoing trials. Bachelor’s degree preferred with 1+ year of clinical research experience.