Lead safety science strategy and delivery for cell therapy assets, integrating clinical, nonclinical, epidemiologic and real-world evidence to shape safety profiles and guide benefit-risk decisions.
Compensation
The annual base pay for this position ranges from $203K to $305K. Our positions offer eligibility for multiple incentives an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.
Responsibilities
Lead safety surveillance, signal detection, validation, evaluation and management for assigned cell therapy assets
Set the safety science strategy for multiple, complex or high-priority assets and translate emerging data into clear recommendations
Lead proactive pharmacovigilance and risk-management planning, including Global Risk Management Plans, REMS, risk-minimization measures and benefit-risk assessments
Provide strategic leadership and oversight for aggregate reports and safety deliverables, including DSURs, PBRERs/PSURs, PADERs, RMPs, REMS and ad hoc analyses
Lead safety content and strategy for protocols, Investigator Brochures, Reference Safety Information, informed consent forms, clinical study reports, Data Monitoring Committee materials and core data sheets
Requirements
Bachelor’s degree in life sciences, pharmacy, nursing or a related discipline
Advanced degree in immunology, autoimmune disease, pharmacology, epidemiology or a related discipline
Nice to have: advanced degree (MSc, PhD, PharmD)
Nice to have: immunology cell therapy development
Nice to have: peri-submission and/or post-marketing safety
Lead safety science activities for cell therapy assets within the Global Patient Safety Unit, integrating data, managing risk, and supporting regulatory submissions.
Compensation
The annual base pay for this position ranges from $132K to $199K. Our positions offer eligibility for multiple incentives an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.
Responsibilities
Conduct and coordinate safety surveillance, signal detection, validation, evaluation and management for assigned cell therapy assets
Develop MedDRA search strategies
Translate emerging safety data into clear analyses and recommendations
Lead components of pharmacovigilance and risk‑management planning
Author and project‑manage aggregate reports and safety deliverables
Requirements
Bachelor’s degree in life sciences, pharmacy, nursing or a related discipline
Advanced degree in immunology, autoimmune disease, pharmacology or a related discipline
Lead safety science activities for cell therapy assets within the Global Patient Safety Unit, integrating data, managing risks, and supporting regulatory submissions.
Compensation
The annual base pay for this position ranges from $132K to $199K. Our positions offer eligibility for multiple incentives an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.
Responsibilities
Conduct and coordinate safety surveillance, signal detection, validation, evaluation and management for assigned cell therapy assets
Develop MedDRA search strategies
Translate safety data into analyses and recommendations
Lead pharmacovigilance and risk‑management planning
Author and project‑manage safety reports and deliverables
Requirements
Bachelor’s degree in life sciences, pharmacy, nursing or a related discipline
Advanced degree in immunology, autoimmune disease, pharmacology or a related discipline
Senior product safety scientist leading SERS programs for the Wellbeing Collective, ensuring safe and compliant innovation through scientific leadership and stewardship.
Compensation
a competitive salary and pension scheme, we also offer an annual bonus, subsidised gym membership, a discounted staff shop and shares.
Responsibilities
Shape priorities: Work with the global Beauty & Wellbeing Head of Product Safety to turn Wellbeing Collective business, R&D and longer-term Wellbeing Collective Horizon 3 science priorities into the wider Beauty & Wellbeing SERS programme.
Deliver innovation plans: Lead SERS input to Wellbeing Collective and Operating Company innovation plans, engaging early to scope projects and set the right level of risk assessment.
Deploy resources well: Plan and coordinate SERS and third-party capability so effort is focused on the highest-value priorities and delivered on time and in full.
Assess and record risk: Ensure safety risks for technologies, products, clinicals, processes and projects are identified, assessed, documented and recorded in SERS digital systems e.g. Pharos for all product safety assessments, to support sound safety decisions.
Provide scientific leadership: Apply deep scientific expertise and judgement to complex consumer safety assessments, innovation programmes and product stewardship decisions.
Requirements
Degree in toxicology, safety science, pharmacology, biochemistry or a related life science
Associate Director, Patient Safety ScientistNewAstraZeneca · Gaithersburg, US