Clinical Trial Associate - Central Monitoring
Octapharma —Lachen, SZ
- Englisch
- Analysefähigkeit
- Patientenversorgung
15 Std.
PhD Candidate / Research Associate in the Field of Data Governance & Digital Value Creation (m/w/d)
Universität St.Gallen —St. Gallen, SG
- 100%
- Informatik
- Doktorat
- Schreibfähigkeiten
3 Tage
PhD Position in Climate-Resilient Walkability and Urban Heat Adaptation
Haute école d'ingénierie et d'architecture de Fribourg —Fribourg, FR
- 100%
- Datenanalyse
- Englisch
- Forschungserfahrung
3 Tage
Shop Manager Geneva
L.Raphael —Genf, GE
- 100%
- Gastgewerbe
- Englisch
- Microsoft Office
Direkt bewerben
3 Tage
Principal, Strategic Advisory Consulting (Life Sciences Supply Chain & Operations)
IQVIA —Basel, BS
- 100%
- Management-Erfahrung
- Englisch
- Master
3 Tage
Senior Director, European Sales (m/f/d)
Molecular Devices —Kloten, ZH
- 100%
- Homeoffice
- Oracle
- Salesforce
- Bachelor
- Bezahlte Ferien
da Vinci Clinical Territory Associate (m/w/d)
Intuitive Surgical —Zürich, ZH
- Homeoffice
- Bis zu 50% Reiseanteil
- Englisch
- Bachelor
12 Std.
Senior Associate - Supply Chain Cyber Security Specialist (Cyber Risk Advisory)
PwC —Zürich, ZH
- 100%
- Englisch
- Master
- Bachelor

More jobs to discover

Find similar jobs that you might be interested in.

Studentische:r Mitarbeiter:in HR Prozessmanagement (m/w/d) - im Stundenlohn
Universität St.Gallen —St. Gallen, SG
40 % (ab sofort oder nach Vereinbarung, befristet bis 31.07.2027). PhD Candidate / Research Associate in the Field of Data Governance & Digital Value Creation (…
14 Tage
Wissenschaftliche:r Mitarbeiter:in/Doktorand:in (m/w/d)
Universität St.Gallen —St. Gallen, SG
PhD Candidate / Research Associate in the Field of Data Governance & Digital Value Creation (m/w/d). Leitung der Gruppe PRS Daten- und Prozessmanagement (m/w/d)…

Ich möchte aktuelle Job-E-Mails für Stellen als associate program erhalten

Wenn Sie sich bei Ihrem Konto anmelden, stimmen Sie den Nutzungsbedingungen, den Richtlinien zur Verwendung von Cookies sowie der Datenschutzerklärung von SimplyHired zu.

Weitere Job-Standorte erkunden

associate program jobs near

Jobs als Clinical Associate in Zürich, ZH

Jobs als Research Associate in Kanton Waadt

Jobs als Clinical Research in Bâle, Bs

Jobs als Research Associate in Basel, Bs

Jobs als Research Associate in Schlieren, Zh

Jobs als Research Associate in Zürich, Zh

Jobs als Payroll Specialist in Zug, Zg

Jobs als Continuous Improvement Specialist in Zürich, Zh

Jobs als Sales Advisor in Flughafen Zürich, Zh

Jobs als Sales Manager in Bern, Be

Jobs als Sales Consultant in Zürich, Zh

Jobs als Technology Innovation Manager in Zürich, Zh

Jobs als Shop Manager in Lausanne, Vd

Jobs als Shop Manager in Zürich, Zh

Jobs als Shop Manager in Winterthur, Zh

Jobs als Product Manager Digital in Zürich, Zh

Jobs als Program Manager in Zürich, Zh

Jobs als Principal Scientist in Spreitenbach, Ag

Jobs als Principal Software Engineer in Zürich, Zh

Jobs als Principal in Baar, Zg

Clinical Trial Associate - Central Monitoring

Octapharma
Lachen, SZ

Jetzt bewerben

Details zur Stelle

Festanstellung
vor 15 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.

Jetzt bewerben

Erweiterte Suche

associate program Jobs

Clinical Trial Associate - Central Monitoring

PhD Candidate / Research Associate in the Field of Data Governance & Digital Value Creation (m/w/d)

PhD Position in Climate-Resilient Walkability and Urban Heat Adaptation

Shop Manager Geneva

Principal, Strategic Advisory Consulting (Life Sciences Supply Chain & Operations)

Senior Director, European Sales (m/f/d)

da Vinci Clinical Territory Associate (m/w/d)

Senior Associate - Supply Chain Cyber Security Specialist (Cyber Risk Advisory)

More jobs to discover

Ich möchte aktuelle Job-E-Mails für Stellen als associate program erhalten

Related Searches

Weitere Job-Standorte erkunden

Your main tasks and responsibilities

Your expertise and ideal skill set

Your department - where you make an impact

Thrive with us

It´s in our blood

Want to find out more about us?

About Octapharma

Tools für Jobsuchende

Arbeitgebertools

Durchsuchen

Bleiben Sie in Kontakt