On-Site Clinical Research Coordinator – 24 hrs/week

IQVIA LLC; Parsippany-Troy Hills (NJ); On-site; USD 48,000 - 58,000; Full time

Job summary

IQVIA LLC is hiring a Clinical Research Coordinator to support clinical studies under the supervision of a principal investigator. On-site in Union, SC, you will perform ECGs, collect samples, assess vitals, and ensure GCP compliance.

Responsibilities include coordinating studies, preparing materials, recruiting and screening participants, and maintaining accurate CRFs. Strong data management and communication skills are essential.

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

ECG

Vital signs

GCP

EDC systems

Data entry

Study coordination

Communication

Education

Bachelor's degree

Tools

EDC systems

Job description

IQVIA LLC is hiring a Clinical Research Coordinator to support clinical studies under the supervision of a principal investigator. On-site in Union, SC, you will perform ECGs, collect samples, assess vitals, and ensure GCP compliance.

Responsibilities include coordinating studies, preparing materials, recruiting and screening participants, and maintaining accurate CRFs. Strong data management and communication skills are essential.