Biotechnology Jobs

• USA - Pennsylvania - Upper Providence
• Hybrid · 2 days in office
• US$222,750 – US$371,250 pa
• Director

Provides clinical and scientific leadership across early and late-stage respiratory programs, designing clinical development plans, protocols and regulatory documents while overseeing medical monitoring and participant safety. Leads a cross-functional Clinical Matrix Team, shaping translational strategy, target validation and evidence generation in partnership with biology, regulatory and commercial groups.

• London
• Director

Provides scientific and medical expertise at study level across early- and late-phase hepatology assets, serving as medical monitor for Phase 1–4 trials and leading protocol, IB, ICF and CSR authoring. Works within cross-functional global study teams and the Clinical Matrix Team, integrating efficacy, safety and biomarker data to inform asset and portfolio decisions, with informal coaching of less experienced clinical scientists.

• 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
• Senior

Monitors clinical trial sites across the UK, performing selection, initiation, monitoring and close-out visits in line with GCP and sponsor requirements. Tracks recruitment, regulatory submissions, CRF completion and data queries, and maintains TMF/ISF documentation. Dedicated to a single sponsor within IQVIA's cFSP model.

Microsoft Word · Microsoft Excel · Microsoft PowerPoint +2

• London
• Hybrid · 3 days in office
• Lead

Owns safety assessment strategy for drug discovery projects from inception to regulatory submission, working with small molecule and biologics platforms. Designs screening cascades, authors IND packages, and manages CRO relationships for outsourced wet-lab work. Also guides development of an AI predictive toxicology platform with ML researchers.

AI/ML · AlphaFold

• London
• Hybrid
• Mid-level

Leads global cross-functional teams to plan, coordinate and deliver regulatory submissions for new marketing authorisations, new indications and other major filings. Manages integrated submission timelines, scenario planning, risk mitigation and forecasts, working with Regulatory Affairs, Clinical, Quality and Manufacturing under the CTD/eCTD framework.

RIMS

• London
• Director · manages people

Lead global labelling strategy for assigned products across early and late-stage development, lifecycle management and marketed portfolios, serving as Therapeutic Area Lead. Drive core labelling documents including CCDS, USPI and EU PI, lead health authority negotiations, and shape a future USPI operating model while championing digitalisation and AI-enabled labelling solutions.

FDA · EMA · ICH

• London
• Director · manages people
• Permanent

Lead the team behind hybrid on-prem and cloud compute infrastructure, Kubernetes clusters, and scientific compute environments supporting ML and drug discovery. Own platform strategy, CI/CD maturity, observability, and security controls for sensitive patient-derived data, reporting to the VP of Engineering.

Kubernetes · Kubeflow · GPU Compute +3

• United Kingdom
• Remote
• Mid-level

Coordinates and oversees clinical trial activities for assigned studies, including regulatory document review, (e)TMF management, and site file compilation. Provides finance support such as raising POs, vendor creation, budget tracking and invoicing using CERPS, Ariba, Fiori and Veeva Payments. Trains new staff and works within a matrixed FSP team.

Veeva Payments · CERPS · Ariba +5

• 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

• 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.

• Southampton
• On-site
• Senior · manages people
• Permanent

Field-based clinical development role leading launch and adoption of pulsed field ablation technologies (VARIPULSE, Dual Energy STSF) across southern UK EP centres. Manages four New Technology Specialists, drives site readiness, first-case support and routine utilisation, and partners with the northern counterpart to set national clinical standards.

CARTO 3 · Biosense Webster · VARIPULSE +1

• Maidenhead
• Senior

Acts as case management subject matter expert for assigned clinical trials, overseeing safety reporting plans, vendor performance and ICSR compliance. Leads pharmacovigilance processes, supports GxP inspections and audits, and provides study-specific training to vendors and internal teams. Requires deep PV and regulatory knowledge in a multinational pharmaceutical setting.

Drug Safety Database