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Job summary
Worldwide Clinical Trials seeks a seasoned Clinical Research Associate to manage site activities across diverse therapeutic areas. You will lead start-up processes, train sites, and oversee regulatory compliance, with regular coaching to advance your career toward Clinical Trial Manager roles. The role emphasizes travel, strong communication, and collaboration with global teams to drive quality outcomes.
Qualifications
Minimum 5+ years of experience as a Clinical Research Associate.
4-year university degree or Nursing degree.
Experience in CNS/Neurology; Psychiatry preferred.
Candidates must reside on the West Coast; travel regionally expected.
Responsibilities
Manage research activities at sites participating in Worldwide’s clinical projects.
Identify potential sites and support start-up activities including regulatory documents and contracts.
Monitor site performance, conduct SIVs, ensure regulatory compliance and safety reporting.
Skills
CRA experience
English communication
Education
Bachelor's or Nursing degree
Tools
CTMS
EDC Systems
Microsoft Office
Job description
Worldwide Clinical Trials seeks a seasoned Clinical Research Associate to manage site activities across diverse therapeutic areas. You will lead start-up processes, train sites, and oversee regulatory compliance, with regular coaching to advance your career toward Clinical Trial Manager roles. The role emphasizes travel, strong communication, and collaboration with global teams to drive quality outcomes.