Biotechnology Jobs

• Rockville, United States
• Hybrid · 2–3 days in office
• US$151,500 – US$252,500 pa
• Director

Leads cross-functional project teams within Oncology Translational Medicine, coordinating diagnostics, biomarker and clinical development activities with internal groups and external labs and manufacturers. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations of diagnostic technologies.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• London
• Mid-level

Mid-level individual contributor on GSK's Enterprise AI Forward Deployed Engineering team, embedded with business unit teams to prototype AI proofs of concept at a days-to-weeks cadence. Works under senior FDEs using AI coding assistants and multi-agent workflows as the default mode of building, then hands proven solutions off cleanly for productionisation.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

• Oxford
• On-site
• Permanent

Builds computational tools and data analysis pipelines for plant biology, working at the intersection of multi-omic analysis and software development. Integrates transcriptomics, metabolomics, proteomics and imaging data, developing pipelines for image segmentation, feature extraction and phenotyping, and preparing datasets for agentic workflows. Collaborates closely with bioinformaticians, research scientists and AI engineers in the Bioinformatics platform team.

• Oxford
• On-site
• £40,000 pa
• Entry level

Develops generative protein design models that capture enzyme dynamics and function, designing conformationally dynamic catalysts. Runs computational and statistical analyses, publishes findings, and collaborates with in vivo evolution teams across the institute. Also mentors PhD students and research assistants and pursues translational and IP opportunities.

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$222,750 – US$371,250 pa
• Director · manages people

Provides clinical and scientific leadership across cardiovascular clinical development programs, designing CDPs, study protocols and regulatory documents while overseeing medical monitoring and participant safety. Leads a cross-functional Clinical Matrix Team, partners with biology, translational sciences, regulatory and commercial groups, and serves as clinical point of contact for regulators, investigators and key experts. Hybrid role with at least two on-site days per week.

• Waltham, United States
• US$195,525 – US$325,875 pa
• Director

Senior individual contributor shaping GSK's Enterprise AI opportunity portfolio across market research, competitive intelligence and knowledge graphs, deciding where forward-deployed engineering pods focus. Involves hands-on prototyping with LLMs and agentic systems, building business cases, defining success metrics and running executive conversations to fund and scale AI products.

IQVIA · Komodo · Reltio +5

• Belgium-Wavre
• Hybrid · 2–3 days in office
• €89,250 – €231,000 pa
• Director

Develops and executes global and regional regulatory strategies for assigned assets in respiratory, immunology and inflammation, managing regulatory interactions, submissions and review processes across major markets. Ensures compliance with internal policies and regulatory requirements to deliver optimal labelling, working closely with global, regional and commercial teams. Hybrid role with mandatory on-site collaboration two to three days per week.

AI

• Rockville Tower Oaks Blvd
• Hybrid · 2–3 days in office
• US$138,600 – US$231,000 pa
• Director

Develops and executes global and regional regulatory strategies for assigned assets in the Respiratory, Immunology & Inflammation therapeutic group, managing regulatory interactions, submissions and review processes across regions. Ensures compliance with internal GSK processes and regulatory requirements to deliver optimal labelling, working closely with global counterparts and commercial teams.

AI

• Durham Blackwell Street
• Hybrid · 2–3 days in office
• US$138,600 – US$231,000 pa
• Director

Develops and executes global and regional regulatory strategies for assigned assets in respiratory, immunology and inflammation, managing regulatory interactions, submissions and review processes across major markets. Ensures compliance with internal GSK processes and regulatory requirements to deliver optimal labelling, working in a matrixed team and liaising with commercial and global counterparts.

AI

• USA - Pennsylvania - Upper Providence
• Hybrid · 2–3 days in office
• US$187,275 – US$312,125 pa
• Director

Leads the scientific design and execution of interventional clinical studies within Medical Affairs, providing medical governance, safety oversight and scientific interpretation of protocols and analysis plans. Collaborates with cross-functional teams, investigators and regulators, and presents results for publications and submissions. Hybrid role with two to three days per week in office.

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$284,250 – US$473,750 pa
• Director · manages people

Leads a team of medical directors and clinical scientists designing and executing early-phase oncology trials, including first-in-human and proof-of-concept studies, while bridging preclinical discovery and clinical development. Accountable for clinical development plans, translational and biomarker strategy, and regulatory submissions across lung and head/neck cancer programmes.

AI/ML · Real World Evidence

• USA - Pennsylvania - Upper Providence
• Hybrid
• US$204,000 – US$340,000 pa
• Director

Leads the design and execution of real-world evidence and health outcomes studies across oncology assets, managing timelines, budgets and vendor deliverables. Reviews protocols, analysis plans and publications, and advises medical, market access and commercial teams on payer and HTA evidence needs. Builds relationships with external experts and maintains knowledge of real-world data sources.

• Baar Onyx
• Hybrid
• US$204,000 – US$340,000 pa
• Director

Leads the design and execution of real-world evidence and health outcomes studies for oncology assets, managing timelines, budgets and quality of protocols, analyses and publications. Advises internal medical, market access and commercial teams and external experts on evidence strategy for HTA submissions, reimbursement and value-based pricing. Requires deep knowledge of RWD sources and payer evidence needs.

• USA - Pennsylvania - Upper Providence
• On-site
• US$242,550 – US$404,250 pa
• Director · manages people

Senior physician leader providing medical oversight, safety monitoring and clinical insight across lung cancer studies, from protocol design through data interpretation. Serves on the Clinical Matrix Team, contributes to regulatory interactions and external scientific engagement, and mentors Medical Directors within the programme. Requires deep lung cancer drug development expertise, including early phase trials.

• USA - Pennsylvania - Upper Providence
• On-site
• US$222,750 – US$371,250 pa
• Director

Serves as the physician within oncology clinical programme teams for lung and head/neck cancers, leading medical monitoring, safety oversight and clinical data interpretation across Phase I–III studies. Partners with a Senior Scientist and cross-functional matrix teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2–3 days per week.

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