Alimentiv

Compensation

Full Description

Job Description: • 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