Jobs in Bristol

Senior SDTM Statistical Programmer

This role involves leading SDTM strategies from protocol review to global regulatory submission, solving complex data integration problems, and mentoring junior programmers. The position is at the forefront of SDTM automation and metadata-driven processes, with a focus on delivering high-impact regulatory filings.

Bristol Myers Squibb Uxbridge

Manager, CMC Documentation

This role involves authoring and coordinating CMC regulatory documents for small molecules, biologics, and ADCs, ensuring they meet global regulatory standards. You'll work closely with cross-functional teams to translate complex scientific data into precise, submission-ready content, and respond to Health Authority inquiries.

Bristol Myers Squibb Wirral

Principal Statistical Programmer

As a Principal Statistical Programmer, you will work closely with cross-functional teams to design and implement technical solutions for clinical data, ensuring accurate and compliant submissions to regulatory authorities. Your role involves hands-on programming, strategic decision-making, and mentoring other technical professionals, all while contributing to life-changing medical advancements.

Bristol Myers Squibb Uxbridge

Associate Director, Global Clinical Science - Neuroscience

This role involves planning, leading, and executing clinical trials in the neuroscience field. Responsibilities include managing trial activities, providing scientific leadership, collaborating with cross-functional teams, and ensuring high-quality data collection and analysis.

Bristol Myers Squibb Uxbridge

Medical Advisor, Cardiovascular

This role involves providing scientific and clinical expertise for cardiovascular therapy, driving UK medical strategy and research plans, and collaborating with various teams. Responsibilities include training the sales force, managing publications, and participating in HTA meetings.

Bristol Myers Squibb Uxbridge

Senior Director, Global Clinical Development (GI Oncology)

This role involves leading the clinical development strategy and execution for one or more indications of a given asset. Responsibilities include designing and overseeing clinical studies, ensuring regulatory compliance, and leading a team of physicians and scientists. The role also involves engaging with external stakeholders and presenting clinical data to governance bodies.

Bristol Myers Squibb Uxbridge

Senior Statistical Programmer

As a Senior Statistical Programmer, you will work within the Global Biometrics & Data Sciences function, writing and validating SAS programs, contributing to regulatory submissions, and collaborating with cross-functional teams. Your role involves hands-on programming, reviewing key planning documents, and leading programming assignments with minimal supervision, directly impacting the development and approval of new medicines.

Bristol Myers Squibb Uxbridge

Senior Manager, Early Clinical Development, Clinical Pharmacology Studies

This role involves designing and providing clinical oversight for early clinical pharmacology studies, from drafting protocols to reviewing clinical data and authoring study reports. You will collaborate with cross-functional teams to ensure the integrity and safety of clinical trials, contributing to the development of innovative treatments.

Bristol Myers Squibb Uxbridge

Associate Director, Biostatistics

The Associate Director of Biostatistics collaborates in the design and execution of clinical trials, contributing to protocol development, statistical analysis, and regulatory submissions. They work closely with cross-functional teams, manage multiple studies, and ensure adherence to standards and quality.

Bristol Myers Squibb Uxbridge

Director, Global Clinical Trial Physician

This role involves leading the design, execution, and oversight of global clinical trials, contributing to the development of innovative medicines. Responsibilities include serving as a scientific authority, shaping clinical development plans, and ensuring data integrity and regulatory compliance.

Bristol Myers Squibb Uxbridge

Principal Scientist, Process Engineering

This role involves working at the intersection of internal science teams and external CDMOs to scale up pharmaceutical processes. Responsibilities include reviewing batch records, assessing CDMO facilities, troubleshooting manufacturing issues, and building strong relationships with partners. The role offers a mix of office work and international travel, with up to 50% remote working flexibility.

Bristol Myers Squibb Wirral