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Clinical Trial Associate - Central Monitoring

Octapharma
Lachen, SZ

Jetzt bewerben

Details zur Stelle

Festanstellung
vor 11 Stunden

Qualifikationen

Englisch
Analysefähigkeit
Patientenversorgung

Vollständige Stellenbeschreibung

Job ID: 61535

Location: Lachen, CH

Job Level: Professionals

Job Category: Research and Development

Employment Type: Permanent position

Career Level:

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.

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

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. Claudia Vignau

Octapharma AG

Seidenstrasse 2, 8853 Lachen

T: +41 55 451 21 35

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.

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