Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Hybrid · 2–3 days in office
• US$149,325 – US$248,875 pa
• Director

Leads epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Designs, oversees and delivers observational and database studies using real-world data, registries and linked sources, and provides scientific advice on study design, analysis plans and interpretation. Manages external vendors, budgets and timelines, and prepares regulatory documents, technical reports and publications.

Electronic Health Records · Claims Data · Registries

• Waltham, United States
• Hybrid · 2–3 days in office
• US$149,325 – US$248,875 pa
• Director

Lead epidemiology programs for one or more assets or disease areas, setting strategy and timelines with clinical development, safety, regulatory, outcomes and commercial partners. Design, oversee and deliver observational and database studies using real-world data, registries and linked sources, while managing external vendors, budgets and timelines and preparing regulatory documents and publications.

Electronic Health Records · Claims Data · Registries

• Cambridge
• Director
• Permanent · Flexible

A senior scientific leadership role shaping and delivering a drug discovery strategy, driving adoption of AI-assisted design, predictive modelling, automation and computational science across a diverse portfolio. The post-holder mentors multidisciplinary teams spanning biology, chemistry, protein design, pharmacology and translational sciences, and acts as a scientific ambassador in client engagements, proposals and partnerships.

• Cambridge
• Lead · manages people

Lead scientific strategy for cardiac electrophysiology and translational ion channel research, acting as scientific lead across multiple integrated drug discovery programmes. Guide experimental design using automated patch clamp (Qube/Sophion), MEA systems and hIPSC-derived cardiomyocytes, while serving as primary client contact and mentoring scientists.

Qube · MEA Systems · Sophion

• Uxbridge
• Hybrid
• Senior · manages people

Technical lead on assigned clinical studies, shaping SDTM strategies from protocol review through to global regulatory submission. Involves root cause analysis, cross-functional collaboration, data integration from CRF and non-CRF sources, and engagement with SDTM automation, metadata-driven processes and agentic AI workflows. Also provides quality oversight to team members and manages CRO and vendor programming activities.

Pinnacle 21

• Uxbridge
• Hybrid
• Lead · manages people

Lead statistical programming for clinical trials, turning complex data into submission-ready outputs using SAS, CDISC, and ADaM standards. Embedded in cross-functional teams, you'll review analysis plans, shape programming strategy, and mentor other programmers while supporting major regulatory filings.

SAS · CDISC · SDTM +2

• 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

• London
• Hybrid
• £130,000 pa
• Senior

Client-facing consulting role in a global technology consultancy's Data & AI practice, serving pharmaceutical and Life Sciences clients. Combines hands-on Data Science, ML and GenAI delivery with strategy, pre-sales and senior stakeholder engagement, focused on commercial applications such as sales, marketing and customer analytics.

Python · SQL

• London
• Hybrid
• Senior
• Permanent

Drive innovation as a strategic consultant on high-impact drug discovery projects with external pharma and biotech partners. Navigate the full development pipeline from target discovery to patient stratification, applying statistical human genetics and large-scale genomic data analysis in R or Python. Partner-facing role translating complex findings into actionable insights.

• United Kingdom
• Remote
• Mid-level · manages people

Lead statistician role delivering analysis database creation, statistical analyses, and formatted tables and summaries with minimal oversight, while mentoring junior team members. Involves leading project teams, interacting directly with sponsors, developing statistical analysis plans and randomization schemes, and programming or validating statistical tables with a strong emphasis on efficacy endpoints using SAS.

SAS · SAS BASE · SAS STAT +2

• Haywards Heath
• Hybrid · 3 days in office
• Director · manages people

Leads a global team of development and regulatory project managers overseeing complex R&D programs across a therapeutic area, including new product development and lifecycle management. Acts as strategic partner to TA and R&D leadership, driving portfolio planning, agile delivery, risk removal and cross-functional alignment as part of the Portfolio & Operations Excellence leadership team.

Microsoft Project · Planview · Smartsheet +1

• Salt Lake City, United States
• Mid-level
• Contract

Develop, optimize and validate cell-based and biochemical assays for automated high-throughput screening, running workflows at scale across 384- and 1536-well formats. Work in a cross-disciplinary team with biologists, automation and data scientists, documenting methods so assays transfer reliably. A 9-month contractor role, Monday to Friday, 9am-5pm.

Liquid Handlers · Plate Readers · Imagers +5

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

Leads cross-functional teams on major EU regulatory submissions (MAA, CTR, IVDR, CTA), health authority interactions with the EMA and national bodies, label negotiations and approvals. Owns the EU engagement strategy, briefing documents and regulatory strategy for oncology programmes, mentoring the Global Regulatory Strategy Team. Distinct for its focus on late-stage oncology assets and European approval pathways.

MAA · CTA · CTR +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

• London
• Lead · manages people

Provides technical leadership in setting up and operating a CDMO site, leading process development and analytical method development projects for cell therapy manufacture. Plans technology transfers, ensures regulatory compliance, drives continuous improvement, and mentors colleagues while engaging directly with clients.

MHRA · EMA · FDA