Related skills
clinical trials statistical analysis risk assessment data quality assurance data monitoring📋 Description
- Lead centralized monitoring to ensure data quality and integrity.
- Develop RBQM plans and conduct study risk assessments.
- Identify KRIs with functional leads and monitor study data.
- Perform centralized statistical monitoring and data review.
- Prepare reports and presentations for sponsors and study teams.
- Mentor junior staff and help document processes.
🎯 Requirements
- Bachelor’s degree in life sciences, statistics, data management, or related field.
- Minimum 2 years in clinical monitoring or trial management.
- Working knowledge of ICH GCP guidelines.
- Strong written and spoken English; excellent communication.
- Proficiency in statistical analysis and data monitoring tools.
- Ability to work independently and in teams.
🎁 Benefits
- Equal Opportunity Employer; diverse candidates welcome.
- Reasonable accommodation available upon request.
- CA Privacy Notice and data protection compliance.
- Privacy policy available on our site.
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