Clinical Research Coordinator - Full-Time

Role Overview: The Clinical Research Coordinator (CRC) supports clinical studies under a principal investigator, performing hands-on procedures, community outreach, and ensuring compliance with protocols and Good Clinical Practice (GCP) guidelines.

Key Responsibilities

• Perform clinical procedures such as ECG, sample collection, and vital signs.
• Coordinate study activities, prepare materials, set up equipment, and manage logistics.
• Recruit, screen, and orient patients, ensuring their safety and well-being.
• Accurately collect and record clinical data in case report forms (CRFs).
• Collaborate with investigators and monitors to address queries and maintain data quality.
• Act as a patient advocate and uphold safety standards according to policies.
  
  

Qualifications & Skills

• Bachelor’s degree preferred or relevant experience.
• At least 1 years of experience in clinical research.
• Knowledge of clinical trials, GCP, and medical terminology.
• Detail-oriented with strong relationship-building skills.
• Proficiency with EDC systems, data entry, and query management.
  
  

Additional Notes: This on-site role is not eligible for sponsorship. Compensation ranges from $35.00 to $42.00 per hour, with potential additional benefits. IQVIA values diversity and is an equal opportunity employer.