Clinical Research Assistant

Job Summary:
We are seeking a detail-oriented Clinical Research Associate with 2–3 years of experience to monitor and manage clinical trials. The ideal candidate will ensure studies are conducted in compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.

Key Responsibilities:

• Conduct site selection, initiation, monitoring, and close-out visits
• Ensure clinical trials are performed in accordance with protocols, SOPs, GCP, and regulatory requirements
• Review and verify source data and case report forms (CRFs)
• Identify, document, and report protocol deviations and safety issues
• Maintain accurate trial documentation and site communication
• Support investigator meetings and training sessions

Qualifications:

• Bachelor’s degree in Life Sciences, Pharmacy, or related field
• 2–3 years of experience as a CRA or similar role
• Strong knowledge of ICH-GCP guidelines and regulatory requirements
• Excellent communication, organizational, and problem-solving skills

Preferred Skills:

• Experience in monitoring multiple sites
• Familiarity with EDC systems
• Ability to travel as required

Pay: $50,000.00 - $60,000.00 per year

Benefits:

• Dental insurance

Work Location: In person