Biotechnology Jobs

• 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$284,250 – US$473,750 pa
• Director

Leads clinical development of GU oncology assets, designing and executing Phase 1-3 interventional trials and serving as a core member of the Clinical Matrix Team. Provides real-time medical monitoring, safety data review with pharmacovigilance, and authors clinical study reports and regulatory responses. Builds key external expert relationships and contributes to business development diligence.

• 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

• Swindon
• Entry level
• Internship

Support the QC Chemistry team by performing routine analytical testing of incoming goods, intermediates and finished products under cGMP conditions. Duties include stock control of reagents and reference standards, equipment checks, calibration and preventative maintenance, reagent preparation, glassware washing, waste disposal and maintaining technical documentation and training records.

pH Meters · Balances

• Swindon
• On-site
• Entry level
• Permanent

Supports the routine running of a QC Microbiology laboratory: booking in samples, maintaining reagent, media and consumable stock, ordering supplies, performing equipment checks and second-analyst checks, and helping clean classified cleanrooms. Also writes and updates SOPs, specifications and scientific reports while working to GMP standards. No previous laboratory experience is required.

Microsoft Word · Microsoft Excel

• Edinburgh
• Lead

Designs, delivers and interprets complex molecular and cellular biology studies for drug discovery and translational research, combining hands-on lab work with technical direction across client programmes. Provides scientific leadership on multiple projects, evaluates new technologies and supports colleagues, working with mammalian cell cultures and advanced cellular systems.

• Maidenhead
• Hybrid · 3 days in office
• US$212,000 – US$251,000 pa
• Director

Leads the full statistical contribution to a clinical development programme, defining statistical strategy for trial design, analysis and regulatory submissions, and representing Biostatistics in interactions with the FDA, EMA and PMDA. Also manages outsourcing to CROs/FSPs and contributes to governance and development-plan decisions across therapeutic areas.

SAS · R

• Maidenhead
• Mid-level

Oversees vendor delivery of medical evaluations for individual case safety reports, applying medical and scientific judgment on causality, expectedness and seriousness. Trains Medical Evaluators, sets assessment frameworks and drives process improvements across Global Safety and Pharmacovigilance. Requires deep pharmacovigilance knowledge and cross-functional stakeholder work.

• Oxford
• On-site
• Senior
• Permanent

Hands-on role developing advanced electronic interfaces, instrumentation and measurement systems for next-generation nanopore sequencing, from proof of concept to integrated multi-channel sensing. Focuses on precision analogue measurement, low-noise picoampere-level circuit design, data acquisition and system integration, working alongside a Senior MEMS Development Engineer and external suppliers.

Nanopore Sequencing · MEMS · Oracle Cloud

• Oxford
• Hybrid
• Permanent

Forward-deployed data engineer embedded with research teams across AI, robotics, biology and pathogen surveillance, turning raw scientific data into reproducible, version-controlled datasets ready for ML. Owns ingestion, storage, curation and transformation of diverse formats (tabular, text, LMDB/Arrow/HDF5, fastq/fasta, cif) and packages pipelines with Docker, Kubernetes, Slurm, Spark or Ray.

Docker · Kubernetes · Slurm +7

• Welwyn
• On-site
• Lead · manages people

Drives and facilitates efficient study start-up for Roche-sponsored clinical trials across the UK, developing start-up strategies and overseeing site activation and regulatory compliance. Engages with Ethics Boards, Health Authorities and CROs, manages budgets and contracts, and champions process automation and team development.

REC · MHRA · HRA

• United Kingdom
• Contract

Shape and drive strategic medical affairs initiatives in the Ophthalmology therapy area, working locally and globally within Roche UK's Medical Affairs Chapter. Involves data and insight generation, scientific partnerships, medical education, and mentoring peers while engaging the clinical community.

• Harrow
• Remote
• Lead · manages people

Acts as functional lead on the core project team, driving site identification and country selection for clinical trials from award onwards. Designs protocol-specific site questionnaires, leads local teams through surveys, models enrolment scenarios, and presents data-driven strategies to sponsors. Also serves as SME for feasibility systems and may lead stand-alone feasibility studies.

• Durham
• £39,560 – £46,970 pa
• Entry level
• Contract

A postdoctoral position investigating whether bacterial enzymes retain post-mortem functions that promote nutrient recycling. The researcher will combine transcriptomics, metabolomics, genetics and large-scale E. coli mutant collections to identify gene products active after death, working in Professor Martin Cann's lab within an interdisciplinary consortium spanning Durham, Edinburgh, Oxford and Cambridge.

Escherichia coli

• Reading
• Senior

Embedded with a global pharmaceutical sponsor, you own end-to-end clinical supply strategy across complex trials: protocol interpretation, label text, demand forecasting, packaging, IRT setup, distribution and temperature-excursion management. You lead vendor oversight, risk assessments and budget tracking while advising study teams and client leadership.

IRT · RTSM · ERP +3