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Senior Clinical Research Associate, CNS
Worldwide Clinical TrialsClinical Research Associate managing research activities at clinical sites for a global CRO. Responsible for compliance, training, and managing all phases of clinical studies.
About the role
Key responsibilities & impact- 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
What you’ll need- 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
Comp & perks- Hands-on, accessible leaders
- Cohesive and supportive teams
- Commitment to cultivating a diverse and inclusive environment
- Professional development opportunities
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchstudy start-up activitiesdata collectionsafety reportingstudy maintenancestudy closurestudy initiation visitsCNSneurology
Certifications
4-year university degreeNursing Degree