Site Management Associate I
ICON · Manila, Philippines
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
ICON seeks a Site Management Associate I to support clinical trial operations in Manila on a hybrid basis. The role involves assisting with site monitoring, protocol compliance, documentation, and cross-functional collaboration to maintain high standards in clinical research delivery.
What they're looking for
- Bachelor's degree in life sciences, healthcare administration, or clinical research
- Strong organizational skills and attention to detail with multitasking ability
- Excellent communication and interpersonal skills for team collaboration
- Basic knowledge of clinical trial processes and regulatory requirements
- Willingness to work hybrid schedule with 2-3 days per week in Makati City
- Clinical research, site management, or related administrative experience preferred
What you'll be doing
- Assist in monitoring clinical trial sites for protocol adherence and GCP guideline compliance
- Prepare documentation, perform data entry, and track site performance metrics
- Collaborate with cross-functional teams to resolve site-related issues and facilitate communication
- Maintain accurate records of site activities and contribute to monitoring report preparation
- Participate in training initiatives to develop clinical trial management knowledge and skills
Privacy & handoff
This role links to ICON'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.