Site Activation Specialist
IQVIA · Pasig, Philippines
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA seeks a Site Activation Specialist to serve as the primary contact for assigned clinical trial sites, managing regulatory compliance, contract negotiations, and project timelines. The role involves coordinating site activities, maintaining internal systems, and ensuring adherence to quality standards and regulatory requirements.
What they're looking for
- Bachelor's degree in life sciences or related field with 3+ years clinical research experience
- In-depth knowledge of clinical systems, procedures, and corporate standards
- Strong negotiation and communication skills with ability to challenge decisions
- Knowledge of GCP/ICH guidelines and applicable regulatory requirements
- Understanding of regulated clinical trial environment and drug development
- Ability to work independently, prioritize tasks, and build effective relationships
What you'll be doing
- Act as single point of contact for investigative sites and serve as Country Lead as applicable
- Prepare and review regulatory documents, site contracts, and budgets for accuracy and completeness
- Maintain internal systems, databases, and tracking tools with project-specific information
- Monitor site performance metrics and ensure adherence to project timelines with contingency planning
- Support regulatory, start-up, and maintenance activities according to applicable SOPs and regulations
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.