Global Clinical Master Data Specialist

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim to prevent stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche where every voice matters.

The Position

A healthier future. Its what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. Thats what makes us Roche.

The mission of the Global Clinical Supply Chain Organisation (PTDS) is to ensure that no patient is left without treatment and no clinical trial is delayed. Our vision is to provide innovative and sustainable clinical supply solutions to anyone anywhere at any time. By joining our team you will play a key role in advancing Roches diverse and robust biopharmaceuticals pipeline encompassing over 100 molecules in approximately 500 clinical trials across seven disease areas in more than 80 countries.

The Opportunity

As our Global Clinical Master Data Specialist you will serve as the backbone of our clinical supply chain ensuring that global production and distribution systems run seamlessly by managing the critical data that fuels our this role your impact and responsibilities will include:

• End-to-End Data Stewardship: Manage GMP/Quality-relevant master data lifecycle processes creating and updating Material Masters Classifications and business partner/vendor data.

• Production Data Management: Oversee production-related data architectures including the precise maintenance of Master Recipes Bills of Materials (BOM) and Production Versions.

• System Integration & Synchronization: Ensure flawless data alignment across SAP R3P Clinical S/4HANA APO and OMP landscapes to fully support global distribution and production planning.

• Lifecycle Governance & Change Management: Lead Engineering Change Management (ECM) workflows and coordinate Engineering Change Requests (ECR) alongside MDGM workflows with global requestors.

• Cross-Functional Collaboration: Partner closely with Production Supply Chain Quality and Pharma Affiliates to successfully translate operational needs into accurate system configurations.

• Technical & Operational Administration: Act as the single point of contact for master data troubleshooting while managing system user accounts and roles via the Corporate Identity Management (CIDM) platform.

• Compliance & Continuous Improvement: Oversee Quality Records within VEEVA (Deviations CAPAs) update SOPs/SPTs and monitor Key Performance Indicators (KPIs) to lead process optimization initiatives.

Who you are

You are a detail-oriented professional with a passion for data integrity within the life sciences looking to make a meaningful impact on global clinical trials. To be successful in this role you bring the following qualifications and skills:

• Educational Background: You possess a University degree in Life Sciences Computer Science Business Administration or a closely related field.

• Industry Expertise: You have a minimum of 5 years of professional experience in Master Data Management with a strong preference for background knowledge in Clinical Supply within the pharmaceutical industry.

• Regulatory Knowledge: You demonstrate a deep foundational understanding of GMP and GCP guidelines ensuring all data meets rigorous corporate and industry quality standards.

• Advanced Technical Proficiency: You are highly skilled in navigating and maintaining complex enterprise systems specifically expert-level knowledge of SAP R3P Clinical S/4HANA MDGM APO and OMP.

• Quality Systems Management: You are proficient with VEEVA platforms possessing the ability to effectively handle Deviations Planned Events and CAPA Records alongside conducting robust root-cause analyses.

• Interpersonal Excellence & Adaptability: You exhibit high cultural awareness coupled with excellent communication skills enabling you to thrive independently or collaboratively while staying calm and proactive under pressure.

• Language Skills: You are fluent in written and spoken English and you ideally bring professional proficiency in German as a significant asset to our global workflows.

Relocation benefits are not available for this job posting.

The expected salary range for this position based on the primary location of Mississauga isand of hiring range. Actual pay will be determined based on experience qualifications and other job-related factors as determined by the company.

We use artificial intelligence to screen assess or select applicants for this role.

This posting is for an existing vacancy at Hoffmann-La Roche Ltd.

Who we are

A healthier future drives us to innovate. Together more than 100000 employees across the globe are dedicated to advance science ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities foster creativity and keep our ambitions high so we can deliver life-changing healthcare solutions that make a global impact.

Lets build a healthier future together.

Roche is an Equal Opportunity Employer.

Required Experience:

IC

Employment Type : Full-Time
Experience: years
Vacancy: 1