Part-Time On-Site Clinical Research Coordinator

IQVIA LLC; Union, Northern (SC, KY); Hybrid; USD 48,000 - 58,000; Part time

Job summary

IQVIA seeks a Clinical Research Coordinator to join our Union, SC team on-site, supporting clinical studies under the supervision of a principal investigator. This role involves hands-on procedures, community outreach, and ensuring high standards of care and compliance.

Ideal candidates have a bachelor’s degree (or equivalent) and at least 1 year of clinical research experience, with knowledge of GCP, data management, and EDC systems. This position emphasizes patient safety and data integrity.

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.
• Strong attention to detail and ability to establish effective working relationships.
• Proficiency with EDC systems, data entry accuracy, and query management.

Responsibilities

• Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
• Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
• Support study conducts by preparing study materials, setting up equipment, and planning logistical activities.
• 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, addressing queries and ensuring data quality.
• Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Skills

GCP principles

Clinical trials knowledge

EDC systems

Data entry accuracy

Query management

Attention to detail

Relationship building

Education

Bachelor’s degree or equivalent

Tools

EDC systems

Job description

IQVIA seeks a Clinical Research Coordinator to join our Union, SC team on-site, supporting clinical studies under the supervision of a principal investigator. This role involves hands-on procedures, community outreach, and ensuring high standards of care and compliance.

Ideal candidates have a bachelor’s degree (or equivalent) and at least 1 year of clinical research experience, with knowledge of GCP, data management, and EDC systems. This position emphasizes patient safety and data integrity.