Biotechnology Jobs

• London
• Hybrid · 2–3 days in office
• €87,000 – €145,000 pa
• Director
• Permanent

Provides medical and scientific expertise in safety evaluation and risk management for GSK assets across clinical development and post-marketing settings. Leads signal detection, periodic regulatory reports, RMPs and benefit-risk assessments within a global cross-functional matrix, presenting complex safety issues to senior governance committees. Distinct for its blend of pharmacovigilance strategy, regulatory writing and matrix leadership.

ICH · GVP · CIOMS

• Belgium-Wavre
• Hybrid · 2–3 days in office
• €87,000 – €145,000 pa
• Director
• Permanent

Provides medical and scientific expertise in safety evaluation and risk management for GSK assets across clinical development and post-marketing settings. Leads signal detection, benefit-risk assessment, regulatory periodic reports and RMPs, and contributes to safety strategy within a global cross-functional matrix. Involves presenting complex safety issues to senior governance committees and mentoring matrix colleagues.

ICH · GVP · CIOMS

• Livingston
• Mid-level · manages people

Supervises a team of laboratory staff in a central laboratory services environment, setting day-to-day operational activities and ensuring effective delivery. Oversees hiring, training, performance management, safety compliance, CAPA and quality incident resolution, and reviews laboratory metrics to drive process improvement. Requires immunology-based clinical laboratory or clinical trials experience and proficiency with LIMS.

LIMS

• London
• Hybrid
• £130,000 pa
• Senior

Client-facing consulting role in a global technology consultancy's Data & AI practice, serving pharmaceutical and Life Sciences clients. Combines hands-on Data Science, ML and GenAI delivery with strategy, pre-sales and senior stakeholder engagement, focused on commercial applications such as sales, marketing and customer analytics.

Python · SQL

• Oxford
• On-site
• Senior

Leads the creation, review and oversight of investigator site budgets and grants across Phase I–IV clinical trials, using Grants Manager/GrantPlan and FMV benchmarking. Manages CRO site budget and CTA negotiations, scenario planning and site activation timelines, with exposure to Generative AI tools for analytics.

Grants Manager · GrantPlan · MS Office +1

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

Lead national medical strategy for the Respiratory & Immunology business unit, spanning inhaled therapies and biologics. Define pre-launch and launch medical plans, drive NHS transforming-care initiatives, and oversee MSL and healthcare delivery teams. Provide scientific leadership across regulatory, market access and real-world evidence work.

NHS · NICE · SMC +3

• Maidenhead
• Mid-level · manages people

Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned projects for content, scientific strategy, timing and tracking, and manages direct reports including hiring, goal-setting and development. Involves guiding cross-functional teams, peer review and maintaining knowledge of ICH and regulatory guidelines.

• Cambridge
• Director · manages people

Leads end-to-end Clinical Systems migration initiatives such as CTMS, eTMF and study startup, from strategy and due diligence through implementation, cutover and legacy decommissioning. Oversees data migration programs, CRO integrations and GxP validation, managing vendors, stakeholders and a team of professionals while shaping the Clinical Systems roadmap.

CTMS · eTMF

• Cambridge
• Director

Leads business process mapping, design and optimisation across CMC Regulatory Affairs, from development and registration through post-approval lifecycle management. Partners with IT, data owners and cross-functional teams to translate regulatory needs into digital, automation and AI use cases, then drives implementation, adoption and KPI measurement. Distinct for combining regulatory operations expertise with AI-enabled capability building in a global matrixed pharma environment.

Veeva Vault · Planisware · Signavio +2

• London
• Remote
• Mid-level

Manages a portfolio of clinical research studies end to end, leading cross-functional teams and client relationships for Patient Cloud products such as eCOA/ePRO, eConsent and virtual trials. Involves risk assessment, study documentation and milestone tracking, with flexibility needed to work American time zones.

MS Office Suite · Google Workspace

• London
• Senior
• Permanent

Builds generative and predictive models of cellular behaviour from high-content imaging, curating cell painting and brightfield datasets and designing evaluation that separates biological signal from technical artefact. Partners closely with ML scientists and wet lab assay teams, linking imaging readouts to single-cell and perturbation data in a matrixed TechBio environment.

NumPy · pandas · Polars +6

• 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

• Oxford
• On-site
• Mid-level

Hands-on automation engineering role supporting drug product packaging and drug substance manufacturing at a new mRNA facility. Involves commissioning and optimising Emerson DeltaV and Allen-Bradley/Rockwell PLC systems, automated labelling and secondary packaging equipment, plus GxP validation, root cause analysis and lifecycle documentation. Works independently as a technical specialist across manufacturing, engineering, quality and digital teams.

Emerson DeltaV · Allen-Bradley · Rockwell Automation +7

• London
• Hybrid
• Director
• Permanent

Lead clinical pharmacology and pharmacometrics across a growing drug discovery portfolio, serving as the quantitative lead on cross-functional project teams. Apply MIDD, PBPK, population PK/PD and QSP modelling to translate nonclinical data into human dosing and trial design, spanning small molecules, biologics and novel platforms. Also manages CRO partnerships and authors regulatory submissions.

NONMEM · R · Monolix +3