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Clinical Trial Manager – Central Monitoring
OctapharmaClinical Trial Manager performing in-depth review of clinical trial data. Managing oversight across multiple studies to ensure compliance and data integrity for a global biopharmaceutical company.
About the role
Key responsibilities & impact- Perform ongoing, in-depth review of clinical trial data across multiple studies (e.g., EDC, IVRS, safety, central laboratory databases)
- Identify data inconsistencies, missing data, protocol deviations, and outliers at patient and site level
- Manage simultaneous data review across multiple small trials, ensuring consistency in oversight
- Review and initiate targeted queries for critical or inconsistent data points
- Provide clear, actionable feedback to avoid repetitive errors
- Detect protocol deviations through data review
- Act as a central point of contact for data-related issues
- Work closely with: Data Management, Biostatistics, Medical Monitoring, and Pharmacovigilance
Requirements
What you’ll need- Strong analytical and clinical judgment
- Ability to connect isolated data points across patients and studies
- High attention to detail
- Effective prioritization across multiple projects
- Comfort with manual and semi-structured data review
Benefits
Comp & perks- Be rewarded with market-related salary and benefits package
- Skills development - We offer various internal and external employee and leadership trainings, trainee programs and digital solutions
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial data reviewdata analysisdata consistency checksprotocol deviation detectionquery initiationdata managementbiostatisticspharmacovigilancesafety data reviewEDC
Soft Skills
analytical judgmentclinical judgmentattention to detailprioritizationcommunicationproblem-solvingcollaborationfeedback provisionorganizational skillsadaptability