Biotechnology Jobs

• Stevenage
• Hybrid
• Senior

Hands-on senior role owning the computerised-system lifecycle for GxP systems, from impact and supplier assessments through validation, release, operation and retirement. Authors and executes CSV documentation, performs data integrity and 21 CFR Part 11 assessments, manages change controls and CAPAs, and supports regulatory inspections as a CSV subject matter expert.

SaaS · Cloud

• Manchester
• On-site
• Entry level

Perform complex clinical procedures such as ECG, phlebotomy, spirometry, cannulation and cardiac telemetry on trial volunteers, and collect and report data per protocol. Support Phase I-IV studies at a hospital-based research facility, ensuring compliance with GCP and SOPs while orienting volunteers and assisting nursing colleagues.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint

• Reading
• Senior

Monitors clinical trial sites across the UK, handling selection, initiation, monitoring and close-out visits in line with GCP and ICH guidelines. Manages multiple protocols, drives subject recruitment, tracks regulatory submissions and CRF data, and maintains Trial Master File documentation. Based in Reading with regular travel to investigative sites.

• Leeds
• Hybrid
• Senior
• Permanent

On-site CRA role monitoring Phase I–Ib studies inside a 100-bed Leeds Clinical Research Unit, covering pre-study, initiation, routine monitoring and close-out visits. Works alongside clinic, pharmacy and lab teams during first-in-human dosing days, using integrated eSource and EDC systems to focus on data integrity and protocol compliance rather than mechanical SDV.

eSource · EDC

• 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

• Abingdon
• Lead
• Permanent

Acts as the single front door between Evotec's Drug Discovery Platforms and the global In Silico & AI organisation, owning demand, relationships and the in silico roadmap. Translates platform science needs across DMPK, ADME/Tox, predictive safety, screening and omics into prioritised AI requirements, then orchestrates delivery across capability units. Carries a commercial mandate, contributing to client proposals, pricing and evidencing value such as margin uplift and cycle time.

• Livingston
• Mid-level · manages people

Supervises a team of laboratory staff in a central laboratory services environment, setting day-to-day operational activities and ensuring effective delivery. Oversees hiring, training, performance management, safety compliance, CAPA and quality incident resolution, and reviews laboratory metrics to drive process improvement. Requires immunology-based clinical laboratory or clinical trials experience and proficiency with LIMS.

LIMS

• United Kingdom
• £55,000 – £70,000 pa

This role involves leading in-vitro toxicology studies within a regulated preclinical environment, focusing on assay development and execution for product safety assessment. The scientist will apply advanced cell-based methods including Neutral Red, Ames, and micronucleus assays, interpret complex biological data, and support regulatory submissions. Collaboration with internal teams and external partners is key, alongside method validation and scientific reporting in a quality-assured laboratory setting.

• 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

• Reading
• Senior

Designs and builds clinical study databases, interpreting protocols and creating eCRF designs, edit specifications and EDC system configurations using CDMS tools aligned to SDTM and CDASH standards. Runs design and edit specification review meetings with data leads, programmers, validation teams, statisticians and clients, while managing multiple concurrent study builds and project financials for programming shared services.

InForm · CDMS

• Macclesfield
• On-site
• Senior
• Permanent

Designs and executes work plans for early drug discovery projects within a Protein Sciences team, supporting multiple projects and presenting results to clients. Hands-on role focused on recombinant protein expression using insect cell systems such as BEVS, S2 and Sf9, including construct design, baculovirus generation and troubleshooting difficult targets like membrane proteins.

BEVS · Sf9 · Sf21 +2

• Maidenhead
• Senior

Lead and manage clinical trial sites across a diverse portfolio spanning oncology, neuroscience, cell & gene and CAR-T therapies. The role emphasises patient safety, data integrity and building trusted relationships with investigators, with autonomy and support for complex, innovative study designs.

• Maidenhead
• Mid-level

Monitors clinical trial sites across a diverse portfolio spanning oncology, neuroscience, general medicine, cell & gene and CAR-T therapy. Leads site management, builds relationships with investigators and study teams, and safeguards patient safety and data integrity on complex, first-in-class studies. Distinct for its breadth across therapeutic areas and advanced therapy exposure rather than a narrow single-indication focus.

• 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.

• London
• Hybrid
• £83,930 – £155,870 pa
• Director

Supports the development, launch and continuous improvement of AI-powered products, working alongside Line Function Product Owners and cross-functional teams to translate product vision and strategy. Manages the product lifecycle from MVP through scaling, tracking budget and value metrics, and collaborating with DDIT and external parties on delivery and handover to maintenance.

Pandas · R