Description

Clinical Trial Manager - Central Monitoring
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.
Join us in shaping our vision to provide new health solutions advancing human life.
Clinical Trial Manager - Central Monitoring
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
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
Your department - where you make an impact
The overall responsibility of the CRD department is to ensure timely and efficient delivery of clinical study results with a continuous focus on patient safety, on compliance with the clinical research guidelines, codes, rules and regulations, and on delivering the clinical data for improved therapeutic options needed for the care of patients worldwide
The Haematology team is based in Lachen, Switzerland, with further team members and coworkers at locations in Austria and USA
You report to the Seni
Thrive with us
You help save lives - Every day is meaningful as we produce life-saving medicines
Family values - Long-term perspective for employees and relationships
Be rewarded with market-related salary and benefits package
You will have a high level of influence where you can make a difference and leave your footprint
Work with skilled and fun colleagues in a relatively informal organization
Skills development - We offer various internal and external employee and leadership trainings, trainee programs and digital solutions
It´s in our blood
We live diversity and stand for equal opportunities as an employer! 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.
Mrs. Vignau
Octapharma AG
Seidenstrasse 2, 8853 Lachen
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Want to find out more about us?
Visit our website Octapharma Career and follow us daily on LinkedIn.
About Octapharma
Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide. jid4386112a jit0625a jiy26a