Biotechnology Jobs

• Manchester
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for clinical trials, ensuring GCP compliance, patient safety and data integrity. Builds relationships with investigators, resolves data queries, mentors junior staff and travels up to 40-60% within the region. Embedded in a sponsor-dedicated functional service partnership model.

Investigator Site Files · Trial Master Files

• Bath
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for a CRO embedded within pharmaceutical sponsor teams, ensuring GCP compliance, patient safety and data integrity. Manages site relationships, recruitment strategies, TMF/ISF documentation and risk escalation, with mentoring of junior staff and up to 40-60% regional travel.

Investigator Site Files · Trial Master Files

• Stevenage
• On-site
• Mid-level
• Permanent

Designs, builds and maintains modular end-to-end data-flows across GSK's R&D division, integrating scattered systems and sources into reusable, machine-readable assets with compliance built into the pipeline. Combines hands-on coding and data specification work with coaching and peer review to raise the team's data-flow standards.

Azure · GCP

• Stevenage
• Lead

Designs, develops and maintains modular end-to-end data-flows across GSK's R&D ecosystem, turning scattered systems and sources into trusted, reusable, machine-readable assets. Embeds compliance-as-code and governance into pipelines, working with metadata ecosystems and agentic solutions on Azure or GCP, and coaches peers on data-flow best practice.

Azure · GCP

• Cambridge
• On-site
• Mid-level · manages people

Lead a medical information operations team, overseeing the development and dissemination of accurate medical and drug information while ensuring regulatory compliance. Responsibilities include supervising staff, quality review of medical/clinical work, client reporting, training, and acting as liaison between clients and program staff. Requires proficiency in English and French.

• Saffron Walden
• Hybrid
• £3,452 – £3,861 pm
• Contract

Develops and maintains Python and Java data pipelines that generate ChEMBL releases, plus other chemogenomics services like SureChEMBL, UniChem and ChEBI. Involves database administration, integrating external chemical databases, and collaborating with interdisciplinary scientists and engineers on curation and quality issues.

RDKit · Open Babel · InChI +7

• Saffron Walden
• Hybrid · 2 days in office
• £3,452 pm
• Mid-level
• Contract

Maintains microbial genomes in Ensembl, loading new annotations, coordinating releases and diagnosing data issues. Develops functional annotation and pangenome pipelines, evaluates taxon-specific annotation tools, and builds Nextflow or Snakemake workflows with Python, relational databases and HPC or cloud infrastructure.

Nextflow · Snakemake · MySQL +7

• United Kingdom
• Remote
• Senior

Acts as independent Principal Investigator overseeing qualitative in-trial research studies, from design through delivery, for pharmaceutical clients. Applies methods like interviews and surveys to capture patient experience data, manages project budgets and timelines, and contributes to proposals and client development. Requires CAQDAS expertise and strong scientific writing.

Atlas.ti · NVivo · MAXQDA +1

• London
• Hybrid
• Senior

Leads global clinical data transparency and disclosure across registries and regulatory platforms such as CTIS, EMA Policy 0070 and Health Canada PRCI, acting as subject matter expert for assigned therapeutic areas. Manages vendor partnerships, FOI access requests, redaction and lay summary work, plus SOP governance, compliance reporting and audit readiness within Global Regulatory Affairs Excellence.

CTIS · ClinicalTrials.gov · EU Clinical Trial Register +3

• 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

• Saffron Walden
• Hybrid
• £38,570 – £49,893 pa
• Senior
• Contract

Develop and apply statistical and deep learning methods to cell-free DNA from pregnant women, calling fetal and maternal genotypes from high-coverage sequence data and building methylation-aware biomarkers for pregnancy complications. Work spans methods development, large cohort application and collaboration with international partners in a statistical genomics group.

Python · R · Unix +6

• Saffron Walden
• Hybrid
• £38,570 – £49,893 pa
• Entry level
• Contract

A postdoctoral research role analysing large-scale human genetic, epigenetic and proteomic datasets, including dried blood spots, birth cohorts and cell-free DNA, to uncover the genetic basis of early-life traits and develop biomarkers for pregnancy and neonatal conditions. The work spans statistical genetics, multi-omics and methods development, with scope to tailor projects to the fellow's interests.

GitHub · Snakemake · Nextflow +1

• Cambridge
• Director · manages people

Leads a team of medical writers and oversees strategic planning and drafting of complex regulatory submissions at the therapeutic area or portfolio level. Acts as subject matter expert, driving document strategy with cross-functional teams across Regulatory Affairs, Clinical Research and Clinical Data Science, plus process improvement and training initiatives.

Workday

• Church Stretton
• Senior

Technical lead role driving innovation in polymeric and silica particle technologies for chromatography, diagnostics and biopharma consumables. Involves independently designing and executing complex polymer synthesis, particle manufacture and surface functionalization, plus technology transfer from lab-scale prototypes to full production. Acts as internal consultant and escalation point for critical materials issues, mentors scientists and shapes long-term technology strategy.

• London
• Hybrid
• Director · manages people

Leads the development and execution of international regulatory strategy across European and Rest of World markets, from first-in-human through post-marketing. Represents Global Regulatory Affairs on core development teams, manages project plans and resources, and advises senior management. Also a people manager within the International GRA leadership team, driving process improvement and regulatory policy engagement.

EMA