Biotechnology Jobs

• Stevenage
• 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. Partners with the Senior Scientist and cross-functional Clinical Matrix Team on protocol development, regulatory interactions and investigator engagement, with on-site presence 2-3 days per week.

AI-enabled insights

• Zug, Switzerland
• 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. Partners with the Senior Scientist and cross-functional teams on protocol development, regulatory interactions and investigator engagement, with on-site presence 2-3 days per week.

AI-enabled insights

• Reading
• Remote
• Senior
• Permanent

Supports Pharmacometrics by programming, validating and delivering NONMEM-ready PK/PD datasets from SDTM/ADaM sources using advanced R, covering pre-lock and post-lock clinical data. Includes QC of datasets from external partners and of custom R packages, plus liaison with Data Management, Biostatistics and Bioanalytical teams and regulatory submission deliverables.

R · NONMEM · SDTM +1

• Cambridge
• Director
• Permanent · Flexible

A senior scientific leadership role shaping and delivering a drug discovery strategy, driving adoption of AI-assisted design, predictive modelling, automation and computational science across a diverse portfolio. The post-holder mentors multidisciplinary teams spanning biology, chemistry, protein design, pharmacology and translational sciences, and acts as a scientific ambassador in client engagements, proposals and partnerships.

• 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

• London
• Hybrid
• Director

Lead CMC regulatory strategy for UK-manufactured and UK-licensed mRNA products across development, registration and post-approval lifecycle. Act as primary point of contact with the MHRA, oversee submissions and manufacturing change assessments, and shape global regulatory approaches across cross-functional matrix teams.

MHRA · Generative AI

• Cambridge
• Director · manages people

Leads end-to-end Clinical Systems migration initiatives such as CTMS, eTMF and study startup, from strategy and due diligence through implementation, cutover and legacy decommissioning. Oversees data migration programs, CRO integrations and GxP validation, managing vendors, stakeholders and a team of professionals while shaping the Clinical Systems roadmap.

CTMS · eTMF

• Uxbridge
• Hybrid
• Senior · manages people

Technical lead on assigned clinical studies, shaping SDTM strategies from protocol review through to global regulatory submission. Involves root cause analysis, cross-functional collaboration, data integration from CRF and non-CRF sources, and engagement with SDTM automation, metadata-driven processes and agentic AI workflows. Also provides quality oversight to team members and manages CRO and vendor programming activities.

Pinnacle 21

• Uxbridge
• Hybrid
• Lead · manages people

Lead statistical programming for clinical trials, turning complex data into submission-ready outputs using SAS, CDISC, and ADaM standards. Embedded in cross-functional teams, you'll review analysis plans, shape programming strategy, and mentor other programmers while supporting major regulatory filings.

SAS · CDISC · SDTM +2

• Ireland
• On-site
• Mid-level · manages people
• Permanent

Manages the people, resources and performance of a 4-on-4-off laboratory shift, owning KPIs such as productivity, error rates, QC pass rate, instrument downtime and sample backlog. Acts as incident lead and primary escalation point for Shift Leads, coordinating with Clinics, Customer Support, IT and Quality to keep testing accurate and within turnaround time.

Microsoft Word · Microsoft Outlook · Microsoft Excel +2

• London
• Hybrid
• £130,000 pa
• Senior

Client-facing consulting role in a global technology consultancy's Data & AI practice, serving pharmaceutical and Life Sciences clients. Combines hands-on Data Science, ML and GenAI delivery with strategy, pre-sales and senior stakeholder engagement, focused on commercial applications such as sales, marketing and customer analytics.

Python · SQL

• London
• Hybrid
• Senior
• Permanent

Drive innovation as a strategic consultant on high-impact drug discovery projects with external pharma and biotech partners. Navigate the full development pipeline from target discovery to patient stratification, applying statistical human genetics and large-scale genomic data analysis in R or Python. Partner-facing role translating complex findings into actionable insights.

• Haywards Heath
• Hybrid · 3 days in office
• Director · manages people

Leads a global team of development and regulatory project managers overseeing complex R&D programs across a therapeutic area, including new product development and life cycle management. Drives portfolio planning, risk assessment, and cross-functional alignment as part of the Portfolio & Operations Excellence leadership team, with hands-on coaching and process improvement.

Microsoft Project · Planview · Smartsheet +1

• Salt Lake City, United States
• Mid-level
• Contract

Develop, optimize and validate cell-based and biochemical assays for automated high-throughput screening, running workflows at scale across 384- and 1536-well formats. Work in a cross-disciplinary team with biologists, automation and data scientists, documenting methods so assays transfer reliably. A 9-month contractor role, Monday to Friday, 9am-5pm.

Liquid Handlers · Plate Readers · Imagers +5