Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Hybrid
• US$123,000 – US$205,000 pa
• Lead

Owns operational delivery of diagnostics across early and late-stage oncology trials, from biosample collection and clinical trial assays at reference and central labs to analysis-ready, audit-ready data. Works in a matrix with strategy, biomarker, clinical operations, data management, regulatory, quality and procurement teams, plus external CROs, labs and vendors, and mentors colleagues as a subject matter expert.

CRO · Central Labs · Reference Labs

• Waltham, United States
• 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 close collaboration across a matrix and deep knowledge of real-world data sources and payer needs.

• Reading
• Remote
• Lead

Provides strategic medical and scientific subject matter expertise in hematology-oncology, advising internal stakeholders on protocol design, clinical development plans and proposals, and supporting client bid-defense meetings. Acts as an internal and external consultant across the research and development lifecycle, coaching project teams and collaborating with business development and operations. Greater independence is expected over time under the therapeutic area head.

• 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

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

Owns the end-to-end sample-to-sequence pipeline for the Trillion Gene Atlas, spanning DNA extraction, library prep and sequencing dispatch across Phase 1 and Phase 2. Bridges R&D and production by scaling validated protocols, applying Lean/Six Sigma to improve throughput, and leading a small lab team while monitoring data return with bioinformatics partners.

Illumina · Ultima · PacBio +3

• London
• Remote
• Senior · manages people

Leads cross-functional clinical trial teams for biotech clients, owning project plans, budgets, P&L, risk management and client relationships from Phase I to III. Requires strong CRO experience and therapeutic expertise in oncology plus areas such as dermatology, women's health, neurology, rare disease or radiopharmaceuticals, working fully remotely within a select EMEA country.

Microsoft Excel · PowerPoint · Microsoft Word +1

• 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.

• Reading
• Mid-level · manages people

Leads end-to-end delivery of regional and global clinical trials embedded within a sponsor's team, managing timelines, budgets, risk and cross-functional groups. Also supports bid defence presentations, vendor management and financial forecasting, mentoring less experienced project team members.

IQVIA

• 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

• Cambridge
• Hybrid
• Mid-level
• Permanent

Educates and trains clinicians on Masimo monitoring technologies, running product demonstrations, evaluations and deployments alongside account managers across the Eastern UK territory. Requires critical care, NICU, PICU or emergency nursing background and involves around 60% travel with overnight stays.

PowerPoint

• High Wycombe
• Entry level
• Internship

Supports the Local Trial Manager and Site Manager with document management and administrative tasks across trial start-up, execution and close-out, ensuring compliance with SOPs and local regulatory requirements. Also contributes to process improvement, training and mentoring of other CTAs, partnering with Business Operations, study teams and stakeholders such as Finance and Procurement.

Microsoft Word · Microsoft PowerPoint · Microsoft Excel

• Slough
• Hybrid · 3 days in office
• £37 – £50 ph
• Contract

Process, analyse and interpret omics data from clinical portfolio studies to uncover biological mechanisms, treatment effects and safety signals. Develop analysis pipelines using state-of-the-art tools, document reproducible code for patient-level data, and write reports and scientific publications. Requires strong bulk and single-cell RNAseq expertise, R, HPC/Unix and Docker skills.

Docker · DNAnexus

• London
• Hybrid
• Lead · manages people

Serves as the clinical trial pharmacy subject matter expert across global oncology programmes, advising on investigational product handling, preparation, storage and accountability, and on hazardous drug and CSTD requirements. Develops pharmacy manuals and training for site pharmacists and study teams, supports audits and CAPAs, and oversees FSP pharmacists and external vendors. Hybrid role spanning London, Paris or Cambridge MA.

Closed System Transfer Devices

• London
• Lead

Ensures clinical trials comply with quality standards, SOPs and health authority regulations, partnering with site management and therapeutic area leads. Builds cluster quality plans, leads CAPA and root cause investigations, and supports audit and inspection readiness across internal and FSP teams. Also handles local regulatory intelligence and supplier quality assessments.

Quality Risk Management System

• Leeds
• Hybrid
• Senior
• Permanent

Leads data management activities across early phase trials, including healthy volunteer and patient populations, multi-site studies and reduced timelines. Accountable for all DM deliverables, resource allocation, client relationships and scope changes, while mentoring the internal study team and adopting new DM technologies.