Clinical Research Coordinator - Savannah, GA

IQVIA•Parsippany, GA

6d•Onsite

About The Position

IQVIA is seeking a Clinical Research Coordinator to support clinical research studies under the supervision of a principal investigator. The on-site role is based in Savannah, Georgia, and is scheduled for 24 hours per week. It involves clinical procedures, community outreach, and maintaining high standards of patient care and regulatory compliance. The coordinator conducts clinical procedures such as ECGs, sample collection, and vital signs; coordinates study activities in accordance with study protocols and Good Clinical Practice (GCP); prepares study materials and equipment; and plans logistics. The role also involves recruiting, screening, and orienting patients, protecting their safety and well-being, collecting and accurately recording clinical data in case report forms (CRFs), collaborating with investigators and monitors to resolve queries and ensure data quality, and advocating for patients while maintaining a safe environment under Health and Safety policies. The position is not eligible for sponsorship. The potential base pay range is $35.00–$42.00 per hour. Actual pay 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, in addition to health, welfare, and/or other benefits.

Requirements

Minimum of 1 year of relevant work experience in clinical research.
Working knowledge of clinical trials, GCP principles, and medical terminology.
Strong attention to detail and ability to establish effective working relationships.
Proficiency with EDC systems, accurate data entry, and query management.

Nice To Haves

Bachelor’s degree, or an equivalent combination of education and relevant experience.

Responsibilities

Perform clinical procedures, including ECGs, sample collection, and vital signs.
Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
Prepare study materials, set up equipment, and plan logistical activities to support study conduct.
Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
Collect and accurately record clinical data in case report forms (CRFs).
Collaborate with investigators and monitors, address queries, and ensure data quality.
Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.