About this role
Role Overview
- Coordinate and facilitate project activities as a Senior Clinical Trial Coordinator
- Provide administrative and technical support to the Project Team
- Proactively communicate any risks to project leads and line manager
- Maintain study specific documentation and global support with specific systems, tools and trackers
- Support scheduling and organization of client and/or internal meetings
- Analyze and reconcile study metrics and findings reports
- Assist with coordination and distribution of Investigator Site File (ISF) to sites
- May attend Kick off meeting and take notes when required
Requirements
- High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification
- Bachelor's degree preferred
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 4 years)
- Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines
- Excellent English language and grammar skills and proficient local language skills as needed
- Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively
- Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
Benefits
- Competitive salary
- Flexible working hours
- Professional development opportunities
- Work from home