Learn about career opportunities, our culture, and our mission to improve human health.
Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management
March 12
🏡 Remote – Anywhere in the UK
Learn about career opportunities, our culture, and our mission to improve human health.
Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management
• Responsible for the clinical operations of a project within a defined regional/global level • Provide oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites • Act as a primary liaison between CRAs and the clinical project team • Develop study tools for site and CRA use • Oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions • Develop training materials and study tools for sites and CRAs
• 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 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 and highly effective interpersonal and organizational skills • Proactive, detail oriented, task-driven and highly organized • Ability to handle multiple tasks to meet deadlines in a dynamic environment
• Home-based • £40,500 - £68,500 a year + Bonus • Accommodations for persons with disabilities are available on request
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