Part-Time Onsite Clinical Research Coordinator (CRC)

Regulatory Jobs; Union (SC); On-site; USD 48,000 - 58,000; Part time

Job summary

IQVIA is seeking a Clinical Research Coordinator to join our on-site Union, SC team. The role involves hands-on clinical procedures, patient recruitment, and ensuring study compliance under the supervision of a principal investigator.

You will support data collection and contribute to high-quality trial conduct. Ideal candidates have at least 1 year in clinical research, knowledge of GCP, and proficiency with EDC systems.

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.
• 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 terminology

Data integrity

Relationship building

Attention to detail

Education

Bachelor's degree or equivalent

Tools

EDC systems

Job description

IQVIA is seeking a Clinical Research Coordinator to join our on-site Union, SC team. The role involves hands-on clinical procedures, patient recruitment, and ensuring study compliance under the supervision of a principal investigator.

You will support data collection and contribute to high-quality trial conduct. Ideal candidates have at least 1 year in clinical research, knowledge of GCP, and proficiency with EDC systems.