Biotechnology Jobs

• Zug, Switzerland
• 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 authority on the Medicine Development Team core quad. Leads governance and investment discussions, Health Authority interactions and evidence-generation strategy, while mentoring clinical development talent and applying AI-enabled analytics to speed decision-making.

AI · Advanced Analytics

• London
• 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 authority within the Medicine Development Team. Leads governance and investment discussions, health authority interactions and evidence-generation strategy, while mentoring clinical development talent and applying AI-enabled analytics to speed decision-making.

AI

• Field Force (England / Wales)
• Hybrid
• £32,690 – £60,710 pa

Site-facing role managing Phase I–IV clinical trial sites, acting as the primary contact between the sponsor and sites. Responsibilities include site initiation visits, training, on-site and remote monitoring, risk assessment and mitigation, and closeout activities, working closely with cross-functional teams to ensure data integrity and compliance.

• Home Worker
• Remote
• £49,140 – £91,260 pa
• Lead · manages people

Leads statistical programming strategy for clinical trials and programs, acting as Trial, Lead or Program Programmer and coordinating internal and external teams. Develops and validates CDISC-compliant datasets and outputs for regulatory submissions, using R, SAS or Python, Git-based version control and reproducible workflows. Also shapes standards, templates and governance across studies.

R Shiny · Tidyverse · Git +2

• Guildford
• On-site
• Entry level
• Permanent

Performs analytical laboratory work on genomics samples, including sample reception, quality control, PCR preparation, and analysis, while ensuring data integrity and compliance with ISO15189 and ISO17025 standards. Maintains equipment, SOPs, training logs, and inventory, reporting issues to the Team Leader. Based in a molecular biology lab on a Monday-to-Friday shift pattern.

LIMS · QMS

• Feltham
• On-site
• Entry level
• Contract

Performs microbiological sample analysis using techniques such as sub-culturing, plate reading, confirmations and validation, running equipment like Vidas and reporting results to customer requirements. Maintains quality records, media QC checks, non-conformance investigations and UKAS/ISO accreditation standards within a team-based laboratory.

Vidas · FGS Software

• Stevenage
• On-site
• Entry level

Support GMP compliance in a multi-product cell and gene therapy facility, reviewing batch manufacturing and QC records, managing controlled documentation, and preparing patient-specific labels. Work with cross-functional teams on batch release, quality events and inspection readiness, on a Sunday–Wednesday shift pattern.

• Reading
• Mid-level

Conducts site qualification, initiation, monitoring and close-out visits for a pharmaceutical sponsor as an embedded member of IQVIA's Clinical Functional Service Partnership team. Monitors patient safety, data integrity and protocol compliance, mentors junior staff, and travels up to 40-60% of the time within the region.

Investigator Site Files (ISF) · Trial Master Files (TMF)

• Stevenage
• On-site
• Entry level
• Shift work

Hands-on manufacturing role producing autologous cell therapies, with roughly 85% of time spent in a GMP cleanroom operating cell-processing equipment, completing documentation and supporting environmental monitoring. Two levels are open: an entry-level Associate Operator and an Operator I for those with GMP or cleanroom experience who take on cell culture, sampling and drug product inspection duties.

GMP Cleanroom · Cell-Processing Equipment

• Cambridge
• Hybrid · 3 days in office
• Director · manages people

Owns International regulatory strategy for complex cell therapy programs, embedding regional requirements into evidence generation, submissions and labeling. Leads BLA/MAA planning, Health Authority engagements and labeling negotiations, integrating clinical, CMC, safety and commercial input. Also leads a matrix regulatory team, coaching colleagues and shaping policy and process improvements.

BLA · MAA · IND +2

• London
• On-site
• £27,500 – £30,000 pa
• Entry level
• Temporary

Processing blood and other biofluids from volunteer donors in a research services lab, including centrifugation, buffy coat and PBMC separation, reagent preparation and microbiological/viral testing of urine. Work follows Human Tissue Act, ISO 9001 and internal safety standards, with responsibility for maintaining laboratory records. Suited to someone starting out who has some blood or accredited lab experience.

• London
• On-site
• Director
• Permanent

Leads CMC regulatory strategy for global submissions including IND, CTA, BLA and MAA, and oversees agency correspondence and compliance for mRNA products. Reviews submissions for readiness, drives health authority interactions, and advises manufacturing and quality teams on change controls and regulatory guidance across vaccines, oncology and rare disease programmes.

IND · CTA · BLA +1

• London
• Remote
• Mid-level

Oversees medical coding activities across clinical studies, managing coding dictionaries such as MedDRA and WHODrug, reviewing coded data for accuracy and compliance, and preparing coding reports for medical review. Acts as subject matter expert, delivering training and partnering with Clinical Development, Pharmacovigilance and Data Management teams to drive process improvements and regulatory compliance.

MedDRA · WHODrug

• Cambridge
• Hybrid · 3 days in office
• Director

Leads an integrated Business Continuity and Crisis Management capability across Oncology R&D, owning the framework, risk registers and BIAs while designing executive-level crisis exercises. Drives emerging-risk assessment, supply-chain nth-tier visibility and the practical use of AI in resilience practice, acting as the audit and regulatory interface for standards such as NIS2.

NIS2 · Business Continuity Software

• 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