Associate Director / Director Safety Scientist

Associate Director / Director Safety Scientist

Associate Director / Director Safety Scientist

Apply locations Welwyn time type Full time posted on Posted 2 Days Ago time left to apply End Date: February 28, 2025 (7 days left to apply) job requisition id 202501-101850

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.

The Position

Join Roche as an Associate Director/Director / Senior Safety Scientist! We’re looking for talented professionals at various experience levels. The position provides safety science and pharmacovigilance support to molecules across the Roche portfolio. As a group, they are responsible for all aspects of safety science/pharmacovigilance, with accountability being held by PCS leadership and experts or SSLs (Safety Strategy Program Leaders) depending on the deliverable/activity.

The Portfolio Safety Scientists (PCS-Sci) supports early and late phase 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:

• 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, but not limited to STAR maintenance, ISMP maintenance. Contribute to the strategy and review of safety assessments and drug safety reports for signals or issues (including product quality) or in response to Regulatory Authority requests.
• Contributing to risk management activities including preparation and maintenance of 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 specialized 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 commercialization 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.

Education, Skills and Experience

• 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.

Who we are

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.

Our UK Pharmaceutical head office is situated in Welwyn Garden City, Hertfordshire, with beautiful countryside surrounding the area. Supported by major motorways & airports as well as being a 30-minute train ride to London, access is easy. Our award-winning office, known as Hexagon Place, was opened in 2005 and provides a modern, flexible working environment with facilities that are second-to-none. Around 2,000 people work at our Welwyn office in Global Early Development (pRED), Global Product Development (PD), Commercial (Rx) and our Corporate functions.

Roche offer a competitive salary plus the excellent benefits you would expect from a blue-chip organisation. There is a fully equipped gym on-site, a library and information centre, and an active sports and social club. We also have a subsidised staff restaurant providing foods to cater for every taste throughout the day. At the heart of the building is an informal meeting area known as The Street which features a coffee shop, snack machine and cashpoint. A second building on-site, called The Hub, contains modern meeting room and conference facilities. Roche promotes personal well-being and work-life balance. Therefore, flexible working options will be considered for all roles at Roche UK.

Roche is committed to creating a diverse & inclusive environment. 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.

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