Biotechnology Jobs

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

Leads a team of medical directors and clinical scientists designing and executing early-phase oncology trials, including first-in-human and proof-of-concept studies, while bridging preclinical discovery and clinical development. Accountable for clinical development plans, translational and biomarker strategy, and regulatory submissions across a lung and head/neck cancer portfolio.

AI/ML

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$284,250 – US$473,750 pa
• Director · manages people

Leads a team of medical directors and clinical scientists designing and executing early-phase oncology trials, including first-in-human and proof-of-concept studies, while bridging preclinical discovery and clinical development. Accountable for clinical development plans, translational and biomarker strategy, and regulatory submissions across lung and head/neck cancer programmes.

AI/ML · Real World Evidence

• Oxford
• On-site
• Entry level
• Permanent

Supports the smooth operation of research laboratories through cleaning, equipment maintenance, calibration and inventory management of reagents and consumables. Acts as point of contact for external servicing visits, handles and transports biological samples, and helps maintain health and safety compliance including waste disposal and temperature-sensitive storage.

• Oxford
• On-site
• Lead · manages people
• Permanent

Build and oversee plant growth and phenotyping facilities, ensuring controlled, reproducible environments in growth chambers and greenhouses. Hands-on player-coach role covering planting, irrigation, pollination, sampling and harvest, plus pest and pathogen management, GMO compliance and phenotype data capture. Also shapes field trial operations and future team hiring.

Controlled Environment Growth Chambers · Greenhouses

• London
• On-site
• Permanent

Runs a high-throughput sample processing pipeline, performing DNA extraction, normalisation and library preparation on soil, faecal and other environmental samples. Operates automated liquid handling platforms such as Myra9, logs everything in Benchling LIMS, and carries out QC checks while supporting R&D protocol testing in a CL2 lab.

Benchling · Myra9 · Hamilton +2

• Abingdon
• On-site
• Director · manages people
• Permanent

Owns Evotec's in silico therapeutics design capability, uniting computational chemistry, generative and modality design (small molecules, peptides, protein engineering, degraders, molecular glues) and predictive ADMET/safety under one mandate. A newly created unit within the In Silico & AI group with an explicit build mandate: set technical vision, grow a multi-site team, and industrialise repeatable, benchmarked methods across partner programmes.

RDKit · Python · AlphaFold

• 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

• Cambridge
• Senior

Acts as subject matter expert for stem cell culture technologies, leading development, optimisation and delivery of cellular systems for drug discovery. Manages multiple cell culture programmes, supplies high-quality cell batches for high-throughput screening, and troubleshoots assays while ensuring biological safety compliance. Collaborates with multidisciplinary teams and external partners across global sites.

Automated Liquid Handling Platforms · High-Throughput Screening

• Cambridge
• Hybrid · 3 days in office
• Director

Provides medical and scientific leadership across late-stage respiratory and immunology clinical programs, from Phase IIb to Phase IV. Involves designing, executing and interpreting pivotal trials, medical monitoring, regulatory document input and building relationships with external scientific experts in an international team.

• Cambridge
• Lead · manages people

Lead multidisciplinary teams defining and delivering AstraZeneca's frontier AI roadmap, turning ambiguous scientific and business questions into scalable AI/ML and agentic systems deployed on cloud and HPC. The role spans problem framing, MLOps, governance and external partnerships, with a strong emphasis on reuse, adoption and measurable scientific impact.

Python · PyTorch · JAX +7

• 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

• United Kingdom
• Remote
• Director · manages people

Senior medical leadership role within a clinical research organisation, acting as a cardiovascular subject matter expert supporting proposals, bid defences and client engagement. Responsibilities span RFP input, protocol and regulatory strategy, internal therapeutic training, and mentoring clinical scientists, with peer-level interaction with pharma medical leadership.

PPD

• United Kingdom
• Remote
• Director · manages people

Senior physician role providing metabolic therapeutic and drug-development expertise to a clinical research organisation, supporting major proposals and bid defences, client peer-to-peer engagement, and protocol design. Also trains and mentors internal clinical teams, authors regulatory documents, and liaises with investigators and KOLs. Requires an MD with metabolic subspecialty certification and fluency in English and Mandarin, with travel to China.

• 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.

• Seqirus USA - NC - Holly Springs
• Lead

Owns quality oversight of external CROs, laboratories and test facilities supporting nonclinical and GLP activities, running the full vendor lifecycle from due diligence and quality agreements to risk-based monitoring, CAPAs and governance forums. Coordinates inspection readiness and audit support, ensures compliance with GLP/GCP/GMP, OECD GLP, 21 CFR Part 58 and ALCOA+ data integrity, and leads vendor risk assessments such as FMEA and risk registers.

OECD GLP · 21 CFR Part 58 · Annex 11 +3