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Senior Clinical Research Associate – CNS
Worldwide Clinical Trials. Manage research activities at sites participating in Worldwide’s clinical research projects .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical research activities, ensuring compliance with regulatory requirements, and conducting study initiation visits. Proficient in utilizing CTMS and EDC systems while maintaining superior organizational and communication skills.
Highest-signal resume keywords
Clinical Research Associate ExperienceCNS/Neurology ExpertiseCTMS ProficiencyEDC Systems ProficiencyRegulatory Compliance Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Research ManagementStudy Initiation VisitsRegulatory Document CollectionContract NegotiationBudget Negotiation
Soft Skills
Interpersonal CommunicationOrganizational SkillsAttention to DetailAbility to Work Independently
Tools & Technologies
Microsoft OfficeCTMSEDC Systems
Certifications & Qualifications
4-Year University DegreeNursing Degree
Industry Keywords
Clinical StudiesInformed ConsentSafety-Event Reporting
About the role
Key responsibilities & impact- Manage research activities at sites participating in Worldwide’s clinical research projects
- Support all stages of clinical studies, including site identification, study start-up, regulatory document collection, contract and budget negotiation, site training, study maintenance, and site closeout
- Conduct study initiation visits (SIVs)
- Ensure compliance with informed consent, safety-event reporting, and applicable regulatory requirements while managing sites remotely
Requirements
What you’ll need- Excellent interpersonal, oral, and written communication skills in English
- Superior organizational skills with attention to detail
- Ability to work with little or no supervision
- Proficiency in Microsoft Office, CTMS, and EDC Systems
- 5+ years of experience as a Clinical Research Associate
- 4-year university degree OR Nursing Degree
- Experience in CNS/Neurology required
- Candidates must reside in the Southeast
- Willingness to travel regionally required
Benefits
Comp & perks- Extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs
- Regular touchpoints and coaching conversations with Line Manager
- Clear career path and professional development toward Clinical Trial Manager roles
- Accessible Executive Leadership team
- Competitive benefits package depending on location