Clinical Research Coordinator (Part-Time) - Patient-Centric

Regulatory Jobs; Novi (MI); On-site; USD 48,000 - 58,000; Full time

Job summary

IQVIA in Novi, MI is seeking a Clinical Research Coordinator to support clinical studies under the supervision of a principal investigator. This on-site role involves hands-on procedures, patient interactions, and ensuring compliance with GCP and study protocols.

Key duties include performing ECGs, collecting specimens, coordinating study activities, recruiting and screening patients, and recording data in CRFs.

Qualifications

• Bachelor's degree or equivalent in a relevant field.
• At least 1 year of clinical research experience.
• Working knowledge of GCP, clinical trials, and medical terminology.
• Experience with prescreening patients.

Responsibilities

• Perform ECG, collect samples, and measure vital signs.
• Coordinate studies and ensure GCP compliance.
• Prepare study materials and set up equipment.
• Recruit and orient patients and ensure safety.
• Record data in case report forms (CRFs).
• Collaborate with investigators and monitors to maintain data quality.
• Advocate for patient safety and maintain a safe environment per policies.

Skills

GCP knowledge

EDC systems

Data entry

Patient recruitment

Clinical procedures

Education

Bachelor's degree preferred

Equivalent experience

Tools

EDC software

Job description

IQVIA in Novi, MI is seeking a Clinical Research Coordinator to support clinical studies under the supervision of a principal investigator. This on-site role involves hands-on procedures, patient interactions, and ensuring compliance with GCP and study protocols.

Key duties include performing ECGs, collecting specimens, coordinating study activities, recruiting and screening patients, and recording data in CRFs.