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

With over 1700 employees, the Octapharma site in Vienna is the largest production site, and successful research and development location.

This position is temporary until 14.07.2028.

Your main tasks and responsibilites

Support the operational execution of global clinical trials, ensuring activities are completed on time and in compliance with ICH-GCP, regulatory requirements, and company procedures
Coordinate study logistics, documentation, systems updates and trial-related tracking activities
Maintain oversight of study records, including (e)TMF management and archiving readiness
Collaborate with cross-functional teams and external partners to support efficient study conduct
Identify operational risks, quality issues, or delays and escalate as appropriate
Contribute to process improvements, training, inspections, audits, and maintenance of procedural documents
Perform other clinical trial administration and operational support activities as assigned

Your expertise and ideal skill set

Medical-pharmaceutical or scientific university degree
At least 5 years experience in clinical research
Previous experience as a Clinical Trials Associate/Assisstant, Clinical Research Associate or similar
Knowledge of the pharmaceutical industry or CRO industry and of the global clinical trials environment
Solid experience with Phase 2 or 3 studies and good IT skills
Proficient in English (written and oral), additional languages beneficial
Strong interpersonal communication and organizational skills
Ability to work efficiently in a team environment and work to tight deadlines

Your department - where you make an impact

We, the Clinical Research & Development department, conduct clinical research to develop new products and ensure their safe and effective use throughout their overall life-cycle. Our ultimate focus in our daily work is on increasing patient health and safety.

Thrive with us

Company restaurant & meal subsidy
Training & further education
Health promotion
Parking spaces and good public transport connections

Enjoy these attractive benefits! You can find all offers here: Benefits

The minimum gross salary according to the collective agreement (chemical industry) is EUR 4.270,14 based on 38 hours per week (full-time). As we strive to offer a salary that reflects your individual profile and qualifications, there is a willingness to pay above the minimum salary.

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.

Do you have any questions? Then get in touch with your contact person.

Mrs. Johanna Proksch, MA

Octapharma Pharmazeutika Produktionsges.m.b.H.

Oberlaaer Straße 235, 1100 Wien

T: +43 (1) 610 32 - 4299

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

regulatory quality management Jobs in wien w

(Senior) Clinical Trial Associate (m/f/d) - temporary

Student Job (f/m/x) - Credit Portfolio Calculations (25 h/week)

Air Traffic Services Training Centre Leader – Europe

VP Research & Development Engineering EMEA

Application Owner – Veeva Platform

Head of Medical Affairs / CRP (m/f/d)

Clinical Trial Lead (m/w/d)

Senior Manager, QSE, CCH

Group Senior Expert (m/f/d) - Fill & Finish

Local Study Associate Director

Associate / Consultant, Vienna

(Sr.) Site Activation Specialist (m/w/d), office-based in Vienna, Austria

Market Access, Pricing & Public Affairs Manager (m/w/d)

Technical Lead (f/m/x) Credit Cards

Application Support Analyst

Senior Clinical Editor

ISO Auditor - Construction Sector (Austria)

Group Senior Expert (m/f/d) - Fill & Finish

Senior Project Director (m/f/d) - Group Project Management

Service Delivery Manager (all genders)

Ich möchte aktuelle Job-E-Mails für Stellen als regulatory quality management in wien w erhalten

Related Searches

Weitere Job-Standorte erkunden

Your main tasks and responsibilites

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