Clinical Research Associate
IQVIA · Pasig, Philippines
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Associate responsible for site monitoring, protocol adherence, and data management for clinical trials. Ensures sites conduct studies per protocol, regulations, and sponsor requirements while managing recruitment, documentation, and quality oversight.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline, or equivalent education and experience
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Strong written and verbal English communication skills
- Organizational and problem-solving abilities
- Ability to build and maintain effective working relationships
What you'll be doing
- Conduct site monitoring visits including initiation, ongoing monitoring, and closeout activities
- Partner with sites on subject recruitment planning and tracking to meet enrollment targets
- Provide protocol training and maintain regular communication with assigned study sites
- Evaluate site compliance with protocol and regulatory requirements; escalate quality concerns
- Track study progress including approvals, enrollment, case report form completion, and data queries
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.