Senior Clinical Research Associate
Worldwide Clinical Trials
full-time
Posted on:
Location Type: Hybrid
Location: Japan
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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 and performing study start-up activities
- Conduct study initiation visits (SIVs)
- Ensure compliance with obtaining informed consent and report potential safety-related events
Requirements
- 2+ years of experience as a Clinical Research Associate
- 4-year university degree or RN/BSN in Nursing
- Experience in Hematology and Oncology is required
- 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
- Willingness to travel required
Benefits
- Health insurance
- 401(k) matching
- Flexible work hours
- Paid time off
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical researchstudy start-up activitiesinformed consentsafety-related eventsHematologyOncology
Soft Skills
interpersonal skillsoral communicationwritten communicationorganizational skillsattention to detailability to work independently
Certifications
4-year university degreeRNBSN