About this role
Role Overview
- Ensuring that sites receive necessary support and engagement issues are resolved
- Being the main client's point of contact for investigative sites
- Accountable for site start-up activities through activation
- Building and retaining investigator site relationships
- Providing support from site recommendation through the lifecycle of studies
- Safeguarding the quality and patient safety at the investigator site
- Contributing to country and site selection activities by proactively collaborating with key stakeholders
Requirements
- Demonstrated experience in site management
- Prior experience as a Clinical Research Associate or Lead CRA
- Demonstrated experience in startup activities through site activation
- Demonstrated experience in conducting and close-out activities
- Demonstrated knowledge of quality and regulatory requirements in applicable countries
- Able to identify and build effective relationships with investigator site staff and other stakeholders
- Proficiency in local language preferred
- English proficiency
- Ability to manage travel as required
Benefits
- Health insurance
- Paid time off
- Professional development opportunities