Part-Time Clinical Research Coordinator – Onsite

IQVIA; Savannah (GA); On-site; USD 48,000 - 58,000; Full time

Job summary

IQVIA in Savannah is seeking a Clinical Research Coordinator to support studies under the supervision of a principal investigator. You will perform hands-on clinical procedures, assist with study materials, and help ensure compliance with GCP and study protocols.

You will recruit and screen participants, collect data for CRFs, and collaborate with investigators to maintain data quality and patient safety throughout the trial.

Qualifications

• Bachelor’s degree or equivalent education/experience.
• At least 1 year in clinical research.
• Working knowledge of clinical trials, GCP, and medical terminology.
• Strong attention to detail and collaborative skills.
• Experience with EDC systems and data queries.

Responsibilities

• Perform clinical procedures and vital signs.
• Coordinate studies and ensure GCP compliance.
• Prepare materials, set up equipment, plan logistics.
• Recruit, screen, and orient patients.
• Record data in case report forms (CRFs).
• Collaborate with investigators and monitors.
• Advocate for patient safety and follow safety policies.

Skills

GCP knowledge

Medical terminology

Attention to detail

Data entry accuracy

Query management

EDC systems

Education

Bachelor's degree or equivalent

Job description

IQVIA in Savannah is seeking a Clinical Research Coordinator to support studies under the supervision of a principal investigator. You will perform hands-on clinical procedures, assist with study materials, and help ensure compliance with GCP and study protocols.

You will recruit and screen participants, collect data for CRFs, and collaborate with investigators to maintain data quality and patient safety throughout the trial.