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The PositionJoin Roche as a Senior Safety Scientist / Associate Director / Director !
We're looking for talented professionals at various experience levels. The position provides hands-on safety science and pharmacovigilance support to molecules across the Roche portfolio. As an individual, they are responsible for all aspects of safety science/pharmacovigilance, with accountability being held by Portfolio Clinical Safety (PCS) leadership and experts or SSLs (Safety Strategy Program Leaders) depending on the deliverable/activity.
The Portfolio Clinical Safety Scientists (PCS-Sci) supports early and late phase molecule development activities as a member of the safety team, providing essential safety oversight and input into all aspects of study management across the entire development and marketed portfolio. In the post-market setting this may include signal evaluation, safety related activities associated with new drug applications/regulatory filings, benefit-risk assessment and safety risk management. A Senior Safety Scientist will be supported by supervision from one or more experienced colleagues but is expected to be able to work unsupervised on less complex deliverables. They will be expected to continue learning about Safety Science/Pharmacovigilance and the broader aspects of drug development.
Key Responsibilities:
Under the matrix leadership of the SSL and/or in collaboration with PCS colleagues develop and maintain an understanding of the safety profile of their assigned product(s) or therapy areas
Responsible for individual and aggregate case reporting activities including ICSR case management (medical review) and aggregate reporting (i.e. DSUR, PBRER)
Responsible for signal detection and management activities including. Contribute to the strategy and review of safety assessments and drug safety reports for signals or issues (inc, product quality) or in response to Regulatory Authority requests
Contributing to risk management activities including preparation and maintenance of Company Core Data Sheet (CCDS), labeling document maintenance, risk communications, RMP, REMS
Contributing to study management from a safety perspective through SMT/PET and document review and maintenance across the development continuum (early phase to post marketing studies), including PASS
Acts independently to manage safety responsibilities on study teams and in activities supporting safety science
Contribute to regulatory authority submissions (Investigational New Drug/IND applications, New Drug Applications/NDAs, Marketing Authorization Applications/MAAs, Variations, Renewals, etc.) by reviewing safety data and preparing relevant sections of the filing and submission packages in consultation with SSL and PCS Team Lead
Participate in and provide input for Drug Monitoring Committees (iDMC) or internal monitoring committee (IMC) meetings, as applicable
Responsible for coordination and collaboration with vendors servicing Safety Science
Take on the responsibility for appropriate specialised roles with PCS. These may include, but are not limited to; functional business process owner, subject matter expert.
Demonstrates behaviors consistent with Roche values and engenders confidence from senior management
Understands how safety activities contribute to company development and commercialisation goals and takes measures to maximize safety value to the organization
Ensures all actions are conducted in alignment with Roche quality management systems
Develop and maintain knowledge of the pharmaceutical industry and drug development, including a comprehensive knowledge of pharmacovigilance activities and requirements
Trains and mentors more junior members of the safety team
Takes on leadership responsibility in order to manage and complete low to medium priority projects
Establish and maintain collaborative working relationships with all key stakeholders, and internal and external customers and ensure the same across relevant teams
Consistently comply with all governing laws, regulations, Roche standard operating procedures (SOPs) and other guidelines
Who you are:
Minimum Qualifications: Qualified healthcare professional or Life Sciences graduate.
Preferred Qualifications: A relevant postgraduate qualification (e.g. PHD/MSc in a Life sciences discipline; Medical qualification; PharmD or other post-graduate health professional qualifications) would be advantageous
Safety scientist (level 2): proven drug safety, clinical development or medical affairs experience in the pharmaceutical or related industry
Understanding of GxP and regulated processes and end to end clinical trial lifecycle
Strong orientation towards process improvement and cross-functional teamwork
Effectively work with remote partners on a global team
Excellent communication skills, both written and verbal
Perform data analysis / statistical methods to evaluate, interpret and present scientific data with clarity
Good presentation skills, effective at summarizing and presenting the key considerations and decision points
Ability to train others on departmental practices and processes
Understanding of project management methodology
Please note the role level will be determined based on experience and demonstrated expertise.
This role is based onsite at our Welwyn, United Kingdom office. Our team follows a hybrid work structure, requiring a fixed number of onsite days per week.
Who we are
A healthier future drives us to innovate. Together, more than 100’000 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.
Let’s build a healthier future, together.
The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.
