Key skills
Communication
About this role
Role Overview
- Responsible for the clinical operations of a project within a defined regional/global level
- Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites
- Acts as a primary liaison between the CRAs and the clinical project team
- Project specific training of CRAs and conducting assessment visits
- Implementation of enrollment and recruitment strategies and preparation of the monitoring plan
- Oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions
- Development of study tools for site and CRA use, review visit reports, review and track protocol deviations
Requirements
- College diploma/degree AND 7-9 years related experience + continuous training and knowledge/skills upgrading
- Undergraduate university degree (Bachelors or Honors Bachelors) AND 4-6 years' experience + substantial on-going job-related training
- Health Sciences, Life Sciences or Nursing specialty preferred, or SoCRA and/or ACRP Certification/Designation
- Minimum of 3 years CRA experience
- Strong experience with EDC systems
- Proficient with MS Office
- Strong written and verbal communication skills
- Highly effective interpersonal and organizational skills
Benefits
- Accommodations for persons with disabilities available on request
- Continuous training and knowledge/skills upgrading