Clinical Trial Manager - Monitoring

Job-: 61535
Location: Lachen, CHE
Job Level: Professionals
Category: Research and Development
Employment Type: Permanent position

• Central Data Review
  • 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.
• Cross-Study Oversight
  • Manage simultaneous data review across multiple small trials, ensuring consistency in oversight.
• Query Management & Data Quality Improvement
  • Review and initiate targeted queries for critical or inconsistent data points.
  • Provide clear, actionable feedback to avoid repetitive errors.
• Protocol Compliance Monitoring
  • Detect protocol deviations through data review.
• Communication & Issue Escalation
  • Act as a central point of contact for data-related issues.
• Collaboration with Functional Teams
  • Work closely with Data Management, Biostatistics, Medical Monitoring, and Pharmacovigilance.

• 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

• Opportunity to help save lives through life‑saving medicines.
• Family values and a long‑term perspective for employees and relationships.
• Market‑related salary and benefits package.
• High influence and opportunity to make a difference.
• Collaborative and informal work environment with skilled colleagues.
• Career development through internal and external training, trainee programs, and digital solutions.

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