Clinical Research Assistant

Benefits

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
• •1 more items(s)

Responsibilities

• •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
• •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
• •5 more items(s)