Biotechnology Jobs

• Waltham, United States
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director · manages people

Provides clinical and scientific leadership across early-phase clinical development programs in GSK's Respiratory, Immunology & Inflammation Research Unit, focusing on aging. Leads the Clinical Matrix Team, designs clinical development plans and study protocols, oversees medical monitoring and safety, and represents programs in regulatory interactions. Works cross-functionally with biology, translational sciences, commercial, and regulatory partners.

• Stevenage
• Hybrid · 2 days in office
• US$189,750 – US$316,250 pa
• Director · manages people

Provides clinical and scientific leadership across translational and clinical studies within GSK's Respiratory, Immunology & Inflammation Research Unit, with a focus on aging. Leads a Clinical Matrix Team, designs clinical development plans and protocols, and oversees medical monitoring, safety and regulatory interactions. Hybrid working with at least two days per week on-site, initially in Stevenage before a planned relocation to Cambridge, UK.

• Lisburn
• Senior · manages people

Senior Statistical Programmer supporting clinical trials within Parexel's FSP team, producing and QCing SDTM and ADaM datasets, tables, figures and listings using SAS. The role can act as Statistical Programming Lead, coordinating global teams, timelines and budgets while liaising with sponsors and Biostatistics and Data Management leads. It also involves mentoring staff and ensuring compliance with ICH-GCP and CDISC standards.

SAS

• Sheffield
• Remote
• Senior

Leads research design and analytical strategies for clinical trials, developing and reviewing statistical analysis plans and authoring reports, abstracts and manuscripts. Acts as functional lead on study teams, directing biostatistical activities, performing complex analyses in SAS or R, and quality-controlling deliverables while mentoring junior staff and liaising with clients on scope and budget.

SAS · R

• London
• On-site
• £57,190 – £106,210 pa
• Lead

Lead all statistical work on assigned neuroscience clinical trials, from protocol development and statistical analysis plans to reporting and exploratory analyses. Drive implementation of innovative trial designs and modern statistical methodologies, collaborating with clinical, regulatory, data management and programming teams to support quantitative decision making.

• London
• Hybrid
• £67,900 – £126,100 pa
• Director · manages people

Lead statistical programming for complex global clinical programs from phase I to IV, coordinating internal and external programmers and setting programming strategy with biostatisticians. Drives adoption of R packages, Shiny applications and AI-enabled tools for visualization and reproducible workflows, while managing resources and acting as functional mentor within the therapy area community.

R · Tidyverse · R Shiny +1

• Maidenhead
• Mid-level

Conducts and oversees site monitoring visits, managing site initiation, monitoring and closeouts while ensuring patient safety, data integrity and GCP compliance. Supports feasibility assessments, investigator recruitment and vendor coordination, and mentors junior team members. Requires Phase I patient-study experience within a client-dedicated FSP team.

• Livingston
• On-site
• Entry level

Assembles clinical trial test kits with specimen collection materials according to protocol, prepares investigator instruction manuals and flowcharts, and packages completed kits with documentation and ancillary supplies for shipment. Monitors inventory levels and alerts supervisors when supplies run low to prevent study delays. Site-based role requiring strong attention to detail and organizational skills.

• Leeds
• Hybrid
• Entry level
• Internship

A student placement supporting the Clinical Operations team in day-to-day coordination of clinical studies, including maintaining the Trial Master File (TMF/eTMF), tracking activities in CTMS, generating reports and distributing study supplies. Based in Leeds with flexibility to work remotely, though onsite working is preferred and may be required.

TMF · eTMF · CTMS +4

• Reading
• Senior

Monitors clinical trial sites across the UK, handling selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines. Manages multiple protocols, drives subject recruitment, tracks regulatory submissions and CRF data, and maintains Trial Master File documentation. Based in Reading with regular travel to investigative sites.

• Cambridge
• Hybrid · 3 days in office
• Lead · manages people
• Permanent

Accountable to the Global Clinical Head for an indication-aligned cluster of late-phase Respiratory and Immunology studies, supervising Global Development Medical Directors and Scientist Directors. Leads cross-functional design, conduct, monitoring and data interpretation, represents the program at health authority interactions, and co-leads publication strategy.

• Maidenhead
• Hybrid
• Mid-level
• Temporary

Monitoring investigator sites across the North of England for a routine post-market surveillance study within a dedicated FSP model. Involves on-site and remote monitoring, building relationships with investigators, and ensuring patient safety, data quality and regulatory compliance, with travel to Oxford at least monthly plus on-site onboarding and training.

• Uxbridge
• Hybrid
• Senior

As a senior individual contributor in the Global Biometrics & Data Sciences function, you write and validate SAS programs to produce derived analysis datasets and clinical Tables, Figures and Listings, and contribute to electronic submission packages such as NDA, BLA and MAA. You also review Statistical Analysis Plans and Data Presentation Plans, partner with external vendors on programming standards, and independently lead programming assignments across multiple projects.

SAS · Pinnacle 21 · MS Office +3

• Oxford
• Hybrid
• Senior

Perform bioanalytical assays using molecular and cellular techniques such as ddPCR, qPCR, RT-qPCR and gel electrophoresis to quantify RNA in biological matrices. Support phase-appropriate assay development, qualification and validation within a GCLP-compliant clinical framework, partnering with internal and external labs and cross-functional teams. The role blends basic science research, bioanalysis and clinical development, with exposure to digital and automation tools.

Droplet Digital PCR · qPCR · RT-qPCR +2

• Welwyn
• Hybrid
• Director

Provides safety science and pharmacovigilance support across the Roche portfolio, covering signal detection, benefit-risk assessment, ICSR case management and aggregate reporting such as DSUR and PBRER. The role also involves preparing CCDS, labelling, RMP and REMS documents and shaping drug safety input into clinical development strategy. Level is set by experience, working with a global team from the Welwyn office.

DSUR · PBRER · CCDS +3