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Senior Clinical Research Associate – Psychiatry
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 effectively training site personnel. Proficient in data collection and reporting, with a strong background in Psychiatry and experience in study start-up and maintenance.
Highest-signal resume keywords
Clinical Research Associate ExperienceStudy Start-Up ActivitiesRegulatory ComplianceMicrosoft Office ProficiencyPsychiatry Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Data CollectionSafety-Event ReportingStudy MaintenanceContract NegotiationBudget Negotiation
Soft Skills
Interpersonal CommunicationOrganizational SkillsAttention to DetailAbility to Work Independently
Tools & Technologies
CTMSEDC Systems
Certifications & Qualifications
4-Year University DegreeNursing Degree
Industry Keywords
Clinical ResearchInformed ConsentGeneral Anxiety DisorderStudy Initiation VisitsMidwestern United States
About the role
Key responsibilities & impact- Manage research activities at sites participating in Worldwide’s clinical research projects
- Identify potential sites to participate in research efforts
- Perform study start-up activities, including collecting regulatory documents and supporting contract and budget negotiations
- Train sites to collect data properly and report potential safety-related events
- Manage site activities during study maintenance
- Close down research activities at sites once the study has concluded
- Conduct study initiation visits (SIVs)
- Ensure compliance with informed consent, safety-event reporting, and applicable regulatory requirements
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 Psychiatry required
- General Anxiety Disorder (GAD) experience a plus
- Candidates must reside in the Midwestern United States
- 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 development that can lead to Clinical Trial Manager roles
- Accessible Executive Leadership team
- Competitive benefits package depending on location