Associate Director / Director Safety Scientist

Roche; Plymouth; On-site; GBP 60,000 - 90,000; Full time

Job summary

Roche is seeking an Associate Director / Director / Senior Safety Scientist to provide safety science and pharmacovigilance support across its portfolio. The successful candidate will oversee case reporting, manage safety responsibilities on study teams, and ensure compliance with Roche quality management systems. We're looking for qualified healthcare professionals or Life Sciences graduates who can contribute to drug safety and the development of life-changing healthcare solutions.

Qualifications

• Proven drug safety, clinical development or medical affairs experience.
• Understanding of GxP and regulated processes.
• Ability to train others on departmental practices.

Responsibilities

• Responsible for individual and aggregate case reporting activities.
• Contributing to risk management activities and regulatory submissions.
• Develop and maintain safety profiles of assigned products or therapy areas.

Skills

Communication

Data analysis

Process improvement

Education

Qualified healthcare professional or Life Sciences graduate

Postgraduate qualification (e.g. PhD/MSc in Life Sciences)

Job description

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

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 and 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, 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 (inc, 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 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

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

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.