Senior Clinical Research Associate
BeOne Medicines
full-time
Posted on:
Location Type: Remote
Location: Italy
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Job Level
Tech Stack
About the role
- Execute clinical monitoring activities and ensure compliance with regulations
- Collaborate with clinical study teams and manage site performance
- Conduct monitoring visits and maintain study documentation
- Mentor junior staff and evaluate site practices
Requirements
- BS in a scientific or healthcare discipline preferred
- At least 3 - 5 years of monitoring experience
- Experience in oncology/onco-hematology trials preferred
- Advanced knowledge of GCP and ICH guidelines
- Excellent communication and interpersonal skills
- Efficient in Microsoft Word, Excel, PowerPoint, Outlook
- Written and verbal communication skills in English
Benefits
- Health insurance
- Flexible work arrangements
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical monitoringmonitoring experienceoncology trialsonco-hematology trialsGCP guidelinesICH guidelines
Soft Skills
communication skillsinterpersonal skillsmentoringevaluation