
Oncology Clinical Monitoring Associate
Há 16 horas
We are seeking an experienced and motivated professional to join our global clinical team as a Clinical Monitoring Associate. This role will be responsible for ensuring the integrity of clinical trials by conducting site visits, monitoring data quality, and maintaining relationships with key site personnel.
Key Responsibilities:
- Conduct site visits to determine protocol and regulatory compliance
- Monitor data quality and patient safety through monitoring and site education
- Build and maintain relationships with key site personnel
Requirements:
- Bachelor's degree in a relevant scientific discipline
- 5+ years of experience in clinical operations or 1+ year as a clinical research associate
- Excellent communication and interpersonal skills
- Fluent in English (writing and speaking)
Benefits:
- Opportunity to work on innovative oncology projects
- Collaborative and dynamic team environment
- Professional development opportunities
Other Information:
- Travel up to 70% may be required
- Proficient in Microsoft Office and industry software
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