Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
Involved in all stages of the clinical study, including identifying potential sites, performing study start-up activities, and supporting negotiation of contracts and budgets
Training the sites to collect data properly and report any potential safety-related events
Managing the site's activities during study maintenance and closing down research activities once the study has concluded
Conduct study initiation visits (SIVs)
Requirements
5+ years of experience as a Clinical Research Associate
4-year university degree OR Nursing Degree
Experience in CNS/Neurology is required
Proficiency in Microsoft Office, CTMS, and EDC Systems
Candidates must reside on the West Coast
Willingness to travel regionally required
Benefits
Hands-on, accessible leaders
Cohesive and supportive teams
Commitment to cultivating a diverse and inclusive environment