Clinical Operations Lead

March 12

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Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management

201 - 500

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 • Develops study tools for site and CRA use, review visit reports, review and track protocol deviations • Contributes to financial project management processes as applicable • Conducts CRA Assessment visits, regular global CRA calls, and meetings with Study Sponsor • Develops training materials and study tools for sites and CRAs, including monitoring plans

Requirements

• 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, highly effective interpersonal and organizational skills • Detail-oriented, task-driven and highly organized • Understanding of GCPs and local regulations as they relate to clinical monitoring • Ability to handle multiple tasks to meet deadlines in a dynamic environment

Benefits

• Home-based • €57,000 - €94,000 a year + Bonus • Accommodations for persons with disabilities are available on request