Biotechnology Jobs

• Waltham, United States
• Hybrid · 2–3 days in office
• US$149,325 – US$248,875 pa
• Director

Lead epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Design, oversee and deliver observational and database studies using real-world data, registries and linked sources, while managing external vendors, budgets and timelines and preparing regulatory documents and publications.

Electronic Health Records · Claims Data · Registries

• London
• Hybrid · 2–3 days in office
• US$149,325 – US$248,875 pa
• Director

Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with cross-functional partners. Designs, oversees and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, data needs and analysis plans. Manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.

Electronic Health Records · Claims Data · Registries

• USA - Pennsylvania - Upper Providence
• Hybrid · 2–3 days in office
• US$151,500 – US$252,500 pa
• Director

Leads cross-functional project teams within Oncology Translational Medicine to advance diagnostic and biomarker development programs, coordinating internal groups and external labs and Dx manufacturers. Manages integrated timelines, budgets, contracts and invoices, tracks milestones and risks, and supports regulatory documentation and technical evaluations. Hybrid role requiring 2-3 days per week onsite.

Microsoft Project · Microsoft Word · Microsoft Excel +7

• Rockville Tower Oaks Blvd
• Hybrid · 2–3 days in office
• US$149,325 – US$248,875 pa
• Director

Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Designs and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, analysis plans and interpretation. Manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.

Electronic Health Records · Claims Data · Registries +1

• Durham Blackwell Street
• Hybrid · 2–3 days in office
• US$149,325 – US$248,875 pa
• Director

Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Designs, oversees and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, data needs and analysis plans. Also manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.

• London

Hands-on role designing, building and maintaining modular end-to-end data-flows across GSK's R&D division, integrating diverse sources into reusable, machine-readable assets with compliance built into the pipeline. Combines technical delivery and coding with coaching and peer review to embed industry best practice, working in a complex matrix environment with varied stakeholders.

Azure · GCP

• UK - Hertfordshire - Ware RD

Designs, builds and maintains modular end-to-end data-flows across GSK's R&D division, integrating diverse sources such as protocol development, DSUR and clinical trial data into a unified machine-readable format. Combines hands-on coding and orchestration with compliance-by-design, documentation and coaching or peer review to embed industry best practice.

Azure · GCP

• UK - Hertfordshire - Ware RD
• On-site
• Lead
• Permanent

Designs and governs modular, end-to-end data-flows for GSK's R&D division, turning scattered systems into reusable, compliance-by-design assets in a machine-readable format. Involves translating business needs into technical data requirements, policy-as-code, metadata ecosystems and agentic solutions, with coaching and peer review across matrix teams.

Azure · GCP

• USA - Pennsylvania - Upper Providence
• US$203,775 – US$339,625 pa
• Director

Provides scientific and strategic leadership for real-world evidence supporting GSK's mRNA vaccine portfolio, with a primary focus on influenza. Leads post-marketing vaccine effectiveness studies in the US, translating evidence needs into rigorous study designs and building collaborations with academic investigators, healthcare systems and data partners. Requires deep expertise in US vaccine effectiveness research, influenza epidemiology, real-world data and causal methods.

Medicare · EHR

• USA - Pennsylvania - Upper Providence
• US$139,425 – US$232,375 pa
• Director

Acts as the operational hub for oncology assets, owning the integrated project plan, budget and risk inputs while driving critical-path acceleration and governance decisions. Partners with project leads to navigate uncertainty, facilitate high-performing teams and embed consistent project management practices across the pipeline.

Planisware · MS Project

• Waltham, United States
• US$139,425 – US$232,375 pa
• Director

Acts as the operational 'COO' of a drug or vaccine asset, owning the single integrated project plan and partnering with project leads to steer strategy through complexity. Drives critical-path acceleration, risk management, governance preparation and cross-functional handoffs, with budget and resource forecasting using tools such as Planisware or MS Project.

Planisware · MS Project

• USA - Pennsylvania - Upper Providence
• Hybrid
• US$123,000 – US$205,000 pa
• Lead

Owns operational delivery of diagnostics across early and late-stage oncology trials, from biosample collection and clinical trial assays at reference and central labs to analysis-ready, audit-ready data. Works in a matrix with strategy, biomarker, clinical operations, data management, regulatory, quality and procurement teams, plus external CROs, labs and vendors, and mentors colleagues as a subject matter expert.

CRO · Central Labs · Reference Labs

• London
• Director

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents the Safety Evaluation & Risk Management function on cross-functional clinical matrix and project teams, escalating emerging safety issues to senior governance. Mentors junior staff and partners with Safety Physicians to shape long-term safety strategy.

• Poznan Grunwaldzka
• PLN 525,750 – PLN 876,250 pa
• Director

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents SERM on cross-functional clinical matrix teams, escalates emerging safety issues to governance bodies and mentors junior staff within a global matrix environment.

• Belgium-Wavre
• €141,000 – €235,000 pa
• Director

Provides advanced scientific expertise in safety evaluation and risk management for key oncology assets in clinical development, leading signal detection, benefit-risk assessment and regulatory safety submissions. Represents SERM on cross-functional clinical matrix teams, escalates emerging safety issues to governance bodies and mentors junior staff within a global matrix.