Biotechnology Jobs

• Waltham, United States
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director · manages people

Owns the clinical strategy, scientific narrative and benefit-risk framework for a genitourinary oncology asset, acting as the senior clinical voice on the Medicine Development Team core quad. Leads governance and investment discussions, Health Authority interactions and evidence-generation strategy, while directing Senior Scientists who handle study-level delivery. Hybrid role with at least two days per week on-site.

AI-enabled Insights · Data Platforms

• Stevenage
• Hybrid · 2 days in office
• US$242,250 – US$403,750 pa
• Director · manages people

Owns the clinical strategy, scientific narrative and benefit-risk framework for a genitourinary oncology asset, acting as the senior clinical voice on the Medicine Development Team core quad. Leads governance and health authority interactions while directing Senior Scientists who handle study-level delivery, and mentors clinical development talent.

AI

• London
• Hybrid
• £49,140 – £91,260 pa
• Lead · manages people

Leads statistical programming strategy across multiple trials or a full program, acting as Trial, Lead or Program Programmer and coordinating internal and external programmers. Develops and validates CDISC-compliant datasets and outputs for CSRs, regulatory submissions and safety reports, using R, SAS or Python, Git-based version control and reproducible workflows. Also shapes standards, templates and governance, with hybrid working from London.

R · SAS · Python +4

• Home Worker
• Remote
• £47,540 – £88,289 pa
• Mid-level

Manages regulatory activities for clinical trial applications across an assigned portfolio, leading high-quality submissions and coordinating responses to Health Authority queries. Works closely with study teams, country leads and cross-functional partners to identify regulatory risks early and secure timely approvals, while contributing to simplification and automation initiatives across Regulatory Affairs.

• Cambridge
• On-site
• Senior
• Permanent

Formulate, dispense and quality-control reagents for a protein discovery platform, operating lab equipment such as pipettes, centrifuges and UPLC systems. The role covers batch documentation, inventory management via ERP and troubleshooting production deviations, working closely with R&D, QA and Supply Chain in a fast-paced lab environment.

UPLC · ERP

• Remote Opportunity - United States
• Remote
• US$261,800 – US$346,060 pa
• Director

Lead clinical pharmacology and pharmacometrics strategy across a portfolio of rare disease and oncology programs, serving as the clinical pharmacology lead and regulatory representative. Oversee modeling and simulation (population PK, PK-PD, exposure-response) and provide pharmacology input on Phase 1-3 study designs. Work cross-functionally with clinical, translational and discovery teams in an end-to-end drug development environment.

WinNonlin · Monolix · NONMEM +1

• Grimsby
• On-site
• Entry level
• Permanent

Analyse food samples using microbiological techniques, including media preparation, plate reading, and result validation, while maintaining UKAS and ISO quality standards. Work a 2-on-2-off shift pattern covering 37.5 hours per week, with responsibility for HSE compliance and liaising with Customer Services on technical matters.

• Grimsby
• On-site
• Entry level
• Permanent

Registration, preparation and analysis of food samples using microbiology techniques, including media preparation, reading plates and validating results. Works to UKAS and ISO quality standards within a shift-based lab team, maintaining records and HSE compliance. Full-time, 37.5 hours per week across two shift patterns.

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review while managing risk-based quality and regulatory compliance. Works within a local study team supporting a key sponsor, with travel across the UK and internationally.

CTMS · eTMF

• London
• Remote
• Senior

Responsible for the successful delivery of clinical studies at assigned investigator sites, acting as the primary point of contact for site management, monitoring, and study execution. Leads site preparation, initiation, routine monitoring, and close-out, conducting onsite and remote visits, source data review and verification, and CRF review. Works within a local study team for a key sponsor, using CTMS, eTMF and risk-based quality management, with travel across the UK and internationally.

CTMS · eTMF

• Huntingdon
• On-site
• Entry level

Performs laboratory-based technical and operational support for in vivo genetic toxicology studies, including the in vivo micronucleus test and COMET assay, under GLP and SOP compliance. Duties cover cell stock maintenance, reagent and media preparation, calibration checks, slide preparation, accurate data recording, QC checks and stock takes, with findings reported to the Study Director.

HASAWA · COSHH

• Reading
• Senior

Conducts site qualification, initiation, monitoring and close-out visits for a dedicated sponsor program, ensuring GCP compliance, patient safety and data integrity. Builds investigator relationships, resolves queries, maintains inspection-ready documentation and mentors junior team members, with up to 40-60% regional travel.

Investigator Site Files · Trial Master Files

• Newcastle upon Tyne
• On-site
• Senior

Leads and coordinates global field action management across Leica Biosystems, including recalls, corrections, removals and Field Safety Corrective Actions. Acts as global process owner and subject matter expert, partnering with Quality, Regulatory, Operations and Commercial teams on investigations, risk assessments and vigilance reporting. Also drives inspection readiness, KPI monitoring and continuous improvement across regions.

EU IVDR · ISO 13485 · FDA +1

• Leeds
• On-site
• Senior

Lead early-phase clinical trials as Principal Investigator or Project Physician, taking studies from start-up through closeout and the Clinical Study Report. Work across first-in-human studies, multiple therapeutic areas and an NHS Trust collaboration, with on-call cover and mentoring of less experienced physicians.

MHRA · cGMP · NHS Trust

• Abingdon
• On-site
• Entry level
• Permanent · Shift work

Operate pilot plant reactors and ancillary equipment in a GMP-regulated large-scale chemical production environment, running multiple syntheses, some never previously scaled. Duties include routine maintenance and reconfiguration of reaction vessels, environmental monitoring, accurate batch documentation, and shift handovers. The role follows a rotating 12-hour day and night shift pattern averaging 42 hours per week.

Microsoft Office