Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.

A healthier future. It’s 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. 

That’s what makes us Roche. 

Please note that this is a 1-year fixed-term role and a CONTRACTOR/CONTINGENT POSITION you will be employed by our 3rd party service provider.

The Opportunity

As a PV Hub Partner, you are responsible for supporting PV activities within the hub coverage areas to ensure PV activities are completed consistently in a timely manner in accordance with internal processes and local and international regulatory requirements. 

Ensures collection, reporting and handling of safety information associated with Roche products is performed according to global Roche and local regulatory requirements within the assigned PV hub coverage areas.

Ensures oversight and management of Individual Case Safety Reports (ICSRs) from all sources in a timely manner, including appropriate follow up, reporting and documentation

Maintains oversight of safety risk management and performs all other PV activities where applicable. 

Proactively manages workload to ensure regulatory timelines are met. 

Strives for excellence in the area of assigned responsibilities and simplification of the processes where possible 

Works in close collaboration with PV Hub process, country champions and Affiliate Patient Safety Partners to maintain compliance of executed activities 

Ensure records are managed as per Coremap requirements 

Who you are

Health Care Professional Degree (e.g. Medical Degree, Pharmacist,) or Life Science Degree (e.g. BSc Biology, BSc Neuroscience, etc.) with appropriate experience in Drug Safety/Pharmacovigilance, preferably 1-2 years

Knowledge of global Pharmacovigilance regulatory requirements 

Ability to evaluate, analyze and interpret data, and draw conclusions, independently  

Fluent in English and German, strong organization skills, detail oriented, ability to adapt to change 

Good interpersonal skills, builds strong sustainable and collaborative relationships with internal and external stakeholders, as well as effective collaboration with functional groups and management 

At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

Roche is an Equal Opportunity Employer.