Senior Clinical Research Associate
Worldwide Clinical Trials
full-time
Posted on:
Location Type: Remote
Location: North Carolina • United States
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Job Level
About the role
- Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
- Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort
- Conduct study initiation visits (SIVs)
- Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements
Requirements
- 5+ years of experience as a Clinical Research Associate
- 4-year university degree or RN/BSN in Nursing
- Excellent interpersonal, oral, and written communication skills in English
- Superior organizational skills with attention to details
- Ability to work with little or no supervision
- Proficiency in Microsoft Office, CTMS, and EDC Systems
Benefits
- health insurance
- inclusive environment that encourages collaboration and creativity
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchstudy initiation visitsinformed consentregulatory compliance
Soft Skills
interpersonal skillsoral communicationwritten communicationorganizational skillsattention to detailability to work independently
Certifications
RNBSN