Clinical Trial Manager - Central Monitoring — Octapharma

NewCHF 96'000 - 146'000
Octapharma · Lachen (SZ)
Categoria: Sanità / Ospedali Contratto: full-time Salario: CHF 96'000 - 146'000
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Location
Lachen
Contract
full-time
Posted
4 days ago
SalaryCHF 96'000 - 146'000

Role overview

Become part of a vital chain and contribute to our common goal of making people’s lives better.

Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines.

We are a privately-owned company, where the warmth of family meets the scale of a global organisation.

Main responsibilities

  • Your main tasks and responsibilities 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 Your expertise and ideal skill set Strong analytical and clinical judgment

Application process

  • We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion.
  • Please apply in English.
  • Do you have any questions?
  • Then get in touch with your contact person.
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Company
Octapharma · Lachen
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