March 12
• Oversight of project deliverables and assigned Clinical Research Associate (CRAs) • Acts as primary liaison between CRAs and clinical project team • Conducts assessment visits with CRAs and implements enrollment and recruitment strategies • Develops study tools for site and CRA use and reviews visit reports • Assures compliance with high-quality and timely project deliverables • Supports other objectives for clinical operations and clinical project team • Provides operational support and guidance to the monitoring team • Develops training materials, study tools, and recruitment strategies • Liaises with line manager for assigning sites to CRAs • Develops presentation materials and presents at various meetings and visits
• College diploma/degree AND 7-9 years related experience + continuous training and knowledge/skills upgrading OR Undergraduate university degree (Bachelors or Honors Bachelors) AND 4-6 years' experience + substantial ongoing 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 • Proactive, detail-oriented, task-driven, and highly organized • Demonstrated understanding of GCPs and local regulations related to clinical monitoring • Ability to handle multiple tasks to meet deadlines in a dynamic environment
• Home-based • Accommodations for persons with disabilities are available on request
Apply Now