Biotechnology Jobs

• Waltham, United States
• US$188,100 – US$313,500 pa
• Director

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Drafts regulatory content for FDA, EMA, CDE, PMDA and ICH submissions, and partners with digital medicine, translational imaging, modelling and data science teams to embed quantitative approaches into asset-level decisions.

MIDD · QSP · AI/ML

• London
• US$188,100 – US$313,500 pa
• Director

Leads end-to-end Model-Informed Drug Development and clinical pharmacology strategy across the drug development lifecycle, from first-in-human studies through filing and lifecycle management. Sits in the Clinical Pharmacology and Quantitative Medicine organisation, partnering with digital medicine, translational imaging, modelling and data science teams, and drafting regulatory content for FDA, EMA and ICH submissions.

MIDD · QSP · AI/ML

• 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

• 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)

• Lisburn
• Senior · manages people

Senior Statistical Programmer supporting clinical trials within Parexel's FSP team, producing and QCing SDTM and ADaM datasets, tables, figures and listings using SAS. The role can act as Statistical Programming Lead, coordinating global teams, timelines and budgets while liaising with sponsors and Biostatistics and Data Management leads. It also involves mentoring staff and ensuring compliance with ICH-GCP and CDISC standards.

SAS

• Harrow
• Remote
• Senior · manages people

Senior Statistical Programmer role focused on R programming for clinical trial analysis and reporting, producing and QCing SDTM/ADaM datasets, tables, figures and listings. The position can act as Statistical Programming Lead, coordinating global teams, managing timelines and budgets, and liaising with sponsors and biostatistics. Dedicated to a single sponsor within an FSP model across UK, Poland, Serbia and Hungary.

R · SDTM · ADaM +1

• United Kingdom
• Remote
• Lead · manages people

Leads global regulatory strategy for Phase 1-4 clinical trials, preparing and assembling CTA submissions and acting as the client-facing liaison with sponsors and regulatory agencies. Represents the regulatory department in bid defense and launch meetings, managing project teams and reviewing clinical and scientific documentation.

Microsoft Word · Microsoft Excel · PowerPoint

• Stevenage
• On-site
• Mid-level

Performs complex sample preparation and quantitative analysis of small molecules and biotherapeutics using instrumentation such as GC-MS, ICP-OES, HPLC and LC-MS, supporting both GMP and non-GMP stability studies. Works largely independently to set up, maintain and troubleshoot analytical instrumentation, interpret data for technical validity and compliance, and report results to client teams. Based full-time onsite at a pharmaceutical client site as part of a functional service provider partnership.

GC-MS · ICP-OES · HPLC +2

• London
• On-site
• Mid-level
• Permanent

Serves as connective tissue across Global Research, Data Science and Science teams, coordinating external sequencing vendors, research partnerships and publication timelines. Owns cross-functional process improvement and tooling oversight, ensuring training data stays synchronised with frontier AI model releases. Reports to the VP of Global Research with dotted-line alignment to the Founding TPM.

Project Management Systems · Lab Management Systems · Data Systems

• United Kingdom
• On-site

Field-based role delivering electro-mechanical hardware support for Roche Diagnostics across the North region, covering troubleshooting, preventive maintenance, modifications and installations at multiple customer sites. Works within the Customer Centric Field Support Team, aligning sales and service and attending customer review meetings. Requires residency in the Yorkshire area.

• United Kingdom

Field-based role maintaining and repairing Roche diagnostic systems across molecular, tissue and serum work areas, using on-site support and remote diagnostics to resolve complex electro-mechanical faults. Responsibilities include preventive maintenance, reporting, customer technical training and regulatory documentation, covering Exeter to Kent or a designated customer base.

Roche Diagnostics Systems · Remote Diagnostic Tools · Digital Portfolio

• Maidenhead
• Hybrid
• Senior · manages people
• Permanent

Technical lead for all data management activities on late phase (IIb-III) clinical trials, from start-up through completion. Develops Data Management and Quality Management Plans, designs CRF/eCRF and database structures, and coordinates edit checks and discrepancy management. Acts as client liaison, tracking cycle times and metrics while overseeing data review staff.

RAVE · EDC

• London
• Hybrid
• £63,917 – £118,703 pa
• Director

Acts as a QA liaison between clinical trial teams and third parties, providing expert support through due diligence, qualification, governance and ongoing monitoring. Focuses on technology-enabled vendors such as digital health tools, medical devices and AI, covering risk assessment, audit support, inspection readiness and escalation of quality issues.

DHT · SaMD · SaaS +1

• London
• £60,000 – £75,000 pa
• Senior · manages people

Lead the UK scientific affairs strategy for an international probiotic and functional food organisation, acting as senior scientific authority. Build KOL relationships across academia and healthcare, oversee human studies and research, ensure claims meet regulations, and manage a scientific affairs team while collaborating with European and global colleagues.

• Cambridge
• On-site
• £20 – £24 ph
• Mid-level
• Temporary

Undertake routine and specialist microbiological and molecular investigations across bacteriology, Containment Level 3, serology, chlamydia and molecular diagnostics, interpreting and reporting results. Operate and maintain automated analysers, manage consumables and lab IT systems, and contribute to quality management, audits and SOP development. Based at Addenbrooke's Hospital within UKHSA's Public Health Microbiology team.

UKAS · HSE