At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune...
At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune...
A Senior Manager, Data Scientist role within Pfizer's Innovation, Data & Analytics (IDA) Team, focused on designing and applying advanced analytical and AI-driven methods to support data-informed decision-making in Medical Affairs. The role involves leading model development, cohort segmentation, and evaluation frameworks while collaborating with engineering, governance, and business stakeholders. It emphasizes methodological rigor, responsible AI use, and translating complex medical and business questions into scalable analytical solutions.
A Senior Manager, Data Scientist role in Pfizer's Innovation, Data & Analytics (IDA) team, focused on designing and applying advanced analytical and AI-driven methods to support Medical Affairs. The role involves leading model development, cohort segmentation, and validation frameworks while collaborating with engineering, governance, and business stakeholders. It emphasizes responsible AI use, real-world healthcare data analysis, and translating complex medical questions into scalable data solutions.
Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.
Lead the development and execution of nonclinical safety strategies for small molecule drug candidates in oncology and non-oncology programs, integrating AI-driven predictive models with traditional toxicology. Build and scale the nonclinical safety function within an AI-first drug discovery environment, ensuring high-quality data feedback to refine computational models. Collaborate across preclinical, clinical, and regulatory teams to advance compounds through IND and NDA/MAA-enabling studies.
Perform on-site installation, maintenance, and repair of advanced medical diagnostic systems in NHS and private laboratories. Provide technical support and troubleshooting for complex laboratory equipment, working closely with lab managers and technicians. The role involves regular weekend work and extensive customer interaction across a diverse range of clinical environments.
Provide on-site service and repair for advanced medical diagnostic systems in NHS and private laboratories, ensuring minimal downtime and optimal performance. Troubleshoot complex technical issues and deliver customer training, working across diverse clinical environments. Role involves frequent site visits and weekend work as part of a five-day, seven-day schedule.
Leads vaccine safety sciences functions, ensuring compliance with pharmacovigilance regulations and global safety standards. Oversees signal detection, safety data analysis, and regulatory documentation while guiding process improvements and cross-functional initiatives. Manages teams and supports regulatory inspections, safety reporting, and the implementation of data visualization tools for enhanced decision-making.
Leads global safety strategy for formulation safety across the product lifecycle, focusing on clinical safety evaluation, signal detection, and risk management. Oversees production of key pharmacovigilance documents and ensures compliance with regulatory standards. Acts as safety representative in cross-functional teams and drives safety specifications and risk mitigation plans.
This role involves leading CMC regulatory strategies for international submissions, including IND/CTA/BLA/MAA filings, with a focus on mRNA-based medicines. The individual will guide global regulatory compliance, interact with health authorities, and support quality and manufacturing teams across therapeutic areas like vaccines, oncology, and rare diseases. It requires deep expertise in biologics CMC regulations and a proactive approach to navigating complex regulatory landscapes.
Leads global regulatory strategy for CMC (Chemistry, Manufacturing, and Controls) in support of mRNA-based medicines, ensuring compliance with international regulations and guiding submissions across multiple therapeutic areas. Works closely with manufacturing, quality, and development teams to prepare high-quality regulatory documentation and engage with health authorities. Focuses on biologics, particularly in vaccines, oncology, and rare diseases, within a rapidly expanding biotech environment.
The Global Program Regulatory Director at Novartis leads the development and execution of global regulatory strategies for innovative medicines. Key responsibilities include guiding Health Authority interactions, evaluating regulatory risks, and leading cross-functional teams to drive successful product development and commercialization.
Manages regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions. Develops strategic regulatory input for safety reports, variations, and renewals, while acting as a liaison with health authorities. Supports global approval processes and contributes to process improvements and team mentorship.
This role involves leading end-to-end clinical supply chain strategy, managing complex global trials, and optimizing logistics and inventory management. You will work closely with cross-functional teams to ensure supply strategies align with trial milestones and commercial readiness.
