Latest Medical Affairs Partner - Nephrology & R Jobs

MSAT Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development to commercial manufacturing. The Molecule Steward ensures product quality, robustness, and manufacturability by leading technical strategy, process optimization, and regulatory compliance across global supply chain teams. The position requires deep scientific expertise, cross-functional collaboration, and leadership in resolving complex technical challenges in a regulated environment.

GSK €103,500 – €172,500 pa

Hybrid Permanent

Privacy Lead – R&D / Chief Patient Office (CPO)

This role involves leading privacy strategy and compliance for R&D and patient-focused initiatives at GSK, ensuring responsible data use in clinical research, digital health, and AI-driven projects. The Privacy Lead embeds privacy-by-design principles, conducts risk assessments, and supports governance across highly regulated environments, balancing innovation with ethical data practices.

GSK

Hybrid Permanent

Senior Director, AI Commercial Business Partner - Biopharmaceuticals Business Unit Europe & Canada

This role involves leading the AI revolution in commercial operations for AstraZeneca's Biopharmaceuticals Business Unit in Europe and Canada. You will act as a translator between business functions and the AI Commercial organization, driving the full lifecycle of AI solutions from ideation to delivery and adoption, ensuring they deliver measurable business impact.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-impact, complex global trials in hepatology, renal, and cardiovascular disease, with a focus on late-phase outcomes studies and rare diseases. The position shapes operational strategy, drives innovation in trial design, and ensures delivery across a diverse asset portfolio. It involves leading vendor partnerships, managing regulatory and quality compliance, and developing clinical teams within a patient-ambitious, data-driven environment.

GSK Stevenage, United Kingdom US$242,550 – US$404,250 pa

Hybrid Permanent

Senior Director, AI Commercial Business Partner - Biopharmaceuticals Business Unit Europe & Canada

This role involves leading AI commercial initiatives and translating business needs into AI use cases for the Biopharmaceuticals Business Unit in Europe and Canada. The Senior Director will work closely with business teams and technical experts to drive the adoption and lifecycle management of AI solutions, ensuring they deliver measurable business impact and enhance customer engagement.

AstraZeneca

Hybrid Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for complex, multi-indication assets in hepatology, renal, and cardiovascular disease, with strategic oversight of global Phase III trials, rare disease programmes, and co-development partnerships. The position involves shaping operational strategy, managing high-level vendor relationships, and driving innovation in trial design including decentralised and hybrid models. It requires leadership in risk management, data-driven decision-making, and team development within a global regulatory and compliance framework.

GSK United Kingdom US$242,550 – US$404,250 pa

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-complexity assets in hepatology, renal, and cardiovascular disease, with a focus on global Phase III outcomes trials, rare disease programmes, and co-development partnerships. The position drives end-to-end operational strategy, including country and site selection, patient recruitment, risk management, and vendor oversight, while ensuring alignment with clinical development and evidence generation plans. It also involves direct leadership of clinical teams, fostering innovation in trial design, and maintaining inspection readiness across the portfolio.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-impact, complex global trials in hepatology, renal, and cardiovascular disease, with a focus on late-phase outcomes studies and rare diseases. The position involves shaping operational strategy, managing CRO partnerships, and driving innovation in trial design while ensuring quality and compliance. Leadership includes direct management of clinical teams and strategic input into asset development across the R&D pipeline.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for complex, high-impact assets in hepatology, renal, and cardiovascular disease, with responsibility for global Phase III trials, rare disease programmes, and co-development partnerships. The position involves setting operational strategy, managing CROs and vendors, driving data-led decision-making, and ensuring trial delivery to time, cost, and quality. It also includes direct leadership of clinical operations teams and integration of innovative trial methodologies.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Senior Director Clinical Operations Asset Lead - Hepatology, renal and cardiovascular disease

This role leads clinical operations for high-complexity assets in hepatology, renal, and cardiovascular disease, with a focus on global Phase III outcomes trials, rare disease programmes, and co-development partnerships. The position drives operational strategy, risk management, and innovation in trial design, while managing senior vendor relationships and developing clinical teams. It emphasizes data-led decision-making, enterprise-wide impact, and compliance across a global development portfolio.

GSK US$242,550 – US$404,250 pa

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also supports site selection, protocol training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Director, Therapeutic Area Biomarker Lead (Neuroscience)

This role involves leading the development and implementation of biomarker strategies for neuroscience drug programs, integrating translational data science, and guiding cross-functional teams through clinical and regulatory processes. The Director will oversee biomarker components in clinical studies, mentor specialists, and ensure regulatory compliance while advancing precision medicine in a collaborative, innovation-driven environment.

Novartis London, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves supporting site selection, protocol training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer United States

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, ensuring data integrity, and supporting site selection and training.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, ensuring data integrity, and supporting site selection and training.

Pfizer

On-site Permanent