Biotechnology Jobs

• Stevenage
• Hybrid · 2 days in office
• US$222,750 – US$371,250 pa
• Director · manages people

Provides clinical and scientific leadership across early-phase cardiovascular programs, shaping clinical development plans, study designs and regulatory documents. Leads a cross-functional Clinical Matrix Team, oversees medical monitoring and safety, and acts as the clinical point of contact for regulators, investigators and key external experts. Hybrid role with at least two days per week on-site.

• Waltham, United States
• Hybrid · 2 days in office
• US$284,250 – US$473,750 pa
• Director · manages people

Leads a team of early clinical development medical directors and clinical scientists, owning Phase I/II clinical development plans including first-in-human, dose-escalation and proof-of-concept studies in lung and head/neck cancers. Bridges preclinical discovery and clinical development, driving translational and biomarker strategy, regulatory submissions and cross-functional matrix teams.

AI/ML

• London
• Hybrid · 3 days in office
• Senior

Research engineers translate frontier research concepts into practical implementations, building and optimising state-of-the-art AI models such as Transformers, GNNs and diffusion models, plus the codebases, data pipelines and infrastructure for training and evaluation. The role sits in an interdisciplinary team of drug discovery experts and ML specialists, with a strong emphasis on experimentation, benchmarking and taking models from conception to production.

JAX · PyTorch · XLA +6

• London
• Hybrid · 3 days in office
• Senior

Operating Partner supporting VPs of AI on high-priority strategic initiatives, acting as a trusted advisor and operational force-multiplier. The role involves translating complex machine learning concepts into executive communications, driving cross-functional alignment without line authority, and unblocking inefficiencies across research, engineering, product and operations in a fast-scaling environment.

AlphaFold

• London
• Hybrid
• Mid-level

Drives clinical supply forecasting and IMP budgeting for global trials, translating study protocols and recruitment projections into forecasting tools and monitoring deviations over 3-12 month horizons. Coordinates cross-functional IMP estimation and risk assessment meetings, aligning manufacturing, packaging and distribution to prevent stock-outs, while leading continuous improvement in a matrixed environment.

RTSM · Excel

• Reading
• Lead

Provides principal-level statistical leadership across Phase II and III clinical trials, independently leading SAP authoring and review while supporting integration activities across studies and programmes. Acts as a proactive statistical partner to clinical, programming and regulatory teams, ensuring compliant, high-quality outputs are delivered on time. Requires strong R programming and immunology therapeutic area exposure is desirable.

R

• London
• Remote
• Mid-level
• Permanent

Field-based medical affairs role acting as a scientific partner to healthcare professionals and thought leaders across the East Midlands, Yorkshire and East of England. Involves non-promotional scientific exchange, medical education, advisory boards, and supporting investigator-sponsored and real-world evidence studies within a neuroscience portfolio, working closely with UK, Ireland and global teams.

ABPI Code

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

Curate molecular interaction and macromolecular complex data from scientific literature and user depositions into the IntAct and Complex Portal knowledgebases. Work with bioinformaticians and developers to build curation workflows combining expert manual curation with AI-assisted literature mining, using ontologies and community data standards.

IntAct · Complex Portal · Gene Ontology +2

• Oxford
• On-site
• Temporary

Serve as engineering owner for GMP manufacturing equipment at Moderna's Harwell facility, supporting the Norwood (MA) network. Provide hands-on floor support, troubleshoot complex mechanical and process issues, lead CAPAs and change controls, and drive continuous improvement and tech transfer for mRNA production. Requires close cross-functional work with equipment SMEs and end users.

TMIX · Single Use Mixers · Buffer Prep Vessels +4

• London
• £47,500 pa
• Entry level
• Contract

Lead an independent research project on eukaryotic cell cycle regulation in the fission yeast model, using cell biology, molecular genetics and biochemistry to study how CDK activity coordinates DNA replication, mitosis and division. The role sits in a collaborative lab and includes scope to develop new approaches and help support PhD students.

Schizosaccharomyces pombe

• 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

• Reading
• Mid-level

Shapes and drives end-to-end clinical trial supply strategy, translating study protocols into kit designs, demand forecasts and packaging plans. Oversees vendors, IRT systems, distribution and temperature-excursion management while leading client and vendor meetings. Combines analytical planning with operational leadership across GxP-regulated clinical supply work.

Interactive Response Technology · Microsoft Word · Microsoft Excel +1

• London
• Remote
• Mid-level

Oversees medical coding activities across clinical studies, managing coding dictionaries such as MedDRA and WHODrug, reviewing coded data for accuracy and compliance, and preparing coding reports for medical review. Acts as subject matter expert, delivering training and partnering with Clinical Development, Pharmacovigilance and Data Management teams to drive process improvements and regulatory compliance.

MedDRA · WHODrug

• London
• On-site
• Entry level
• Internship

A 12-month industrial placement supporting in vivo pharmacology research within Pfizer's Internal Medicine Innovation Centre. Day-to-day work includes rodent husbandry and welfare, non-surgical procedures under a Home Office licence, ELISAs and in vitro potency assays for biologics, all under an experienced Research Director. Distinct for its strong focus on animal welfare and the 3Rs.

ELISA

• London
• On-site
• Entry level
• Internship

A 12-month industrial placement in Pfizer's Peptide Drug Product Development group, working alongside formulation scientists and analytical chemists. The role involves preparing and evaluating peptide formulations, running solubility and stability studies, and gaining hands-on experience with HPLC/UPLC and biophysical characterisation methods.

HPLC · UPLC