Latest Therapeutics Jobs

Isomorphic Labs logo

Head of External Drug Discovery Operations, London

Lead all externalised drug discovery and preclinical lab operations, building and scaling a global CRO infrastructure for an AI-first drug design platform. Oversee experimental throughput, data QC and turnaround times, embed data-generation-by-design standards, and manage vendor governance, budgets and a team of CRO Scientific Leads, Operations Managers and Compound Managers.

Hybrid
GSK logo

Antibody Discovery Associate Scientist

Lab-centric role focused on antibody and protein discovery, integrating yeast-based and phage display selection platforms with in silico design tools. The scientist designs and executes experiments, engineers antibody libraries for therapeutic properties, and may use B-cell sorting, NGS and in vivo approaches within matrix teams. Predominantly lab-based with scientific communication and non-lab workstreams.

GSK Stevenage
GSK logo

Director - Diagnostic Execution (Oncology Translational Medicine)

Provides operational leadership for diagnostic activities across GSK's Antibody Drug Conjugate portfolio, managing a team of Diagnostic Delivery Leads. Accountable for executing biomarker and diagnostic strategies, overseeing external testing partners, vendor selection and diagnostic milestones to support clinical development, regulatory submissions and diagnostic approvals, with drug-diagnostic co-development.

GSK Stevenage
Isomorphic Labs logo

Research Lead (Formulation Sciences), London

Lead formulation strategy for small molecules across drug discovery and preclinical development, designing technologies such as solid dispersions and co-crystals to improve solubility, stability and manufacturability. Work within an interdisciplinary team alongside AI/ML drug design platform groups, managing external CRO resources and authoring regulatory submissions.

Hybrid

Chief Scientist, Modern Drug Discovery

A senior scientific leadership role shaping and delivering a drug discovery strategy, driving adoption of AI-assisted design, predictive modelling, automation and computational science across a diverse portfolio. The post-holder mentors multidisciplinary teams spanning biology, chemistry, protein design, pharmacology and translational sciences, and acts as a scientific ambassador in client engagements, proposals and partnerships.

IQVIA Cambridge
Permanent Flexible

Regulatory Strategy Director, Renal

Lead global regulatory strategy for renal therapy programs across all development phases, serving as the regulatory representative on cross-functional teams. Drive major submissions such as INDs, NDAs, BLAs and MAAs, and lead health authority interactions, while mentoring regulatory team members. Distinct for its international scope and focus on renal, nephrology and rare disease assets.

Vertex Pharmaceuticals London
Hybrid

Senior Director, Intl Regulatory Affairs Geo-Expansion

Leads the development and execution of international regulatory strategy across European and Rest of World markets, from first-in-human through post-marketing. Represents Global Regulatory Affairs on core development teams, manages project plans and resources, and advises senior management. Also a people manager within the International GRA leadership team, driving process improvement and regulatory policy engagement.

Vertex Pharmaceuticals London
Hybrid

Senior Scientist

Drive innovation as a strategic consultant on high-impact drug discovery projects with external pharma and biotech partners. Navigate the full development pipeline from target discovery to patient stratification, applying statistical human genetics and large-scale genomic data analysis in R or Python. Partner-facing role translating complex findings into actionable insights.

Genomics London
Hybrid Permanent

Senior Clinical Data Manager - FSO

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.

Fortrea Maidenhead
Hybrid Permanent

Senior Regulatory Affairs Consultant - Labelling Strategy (home or office based)

Acts as principal labelling strategist within Global Regulatory Affairs, driving development and maintenance of dCCDS, CCDS, USPI and EU SmPC documents across an assigned product portfolio. Leads Global Labeling Committee reviews of proposed label exceptions and represents labelling on regulatory strategy teams, working with safety, clinical and commercial stakeholders. Home or office based across European locations.

Parexel Harrow
Remote

Senior Manager, Early Clinical Development, Clinical Pharmacology Studies

Designs and provides clinical oversight for early-phase clinical pharmacology studies, from drafting protocols and informed consent documents to reviewing data and authoring study reports. Partners with cross-functional teams and external sites across immunology, cardiovascular, haematology and oncology, contributing to regulatory submissions such as INDs and IBs.

Bristol Myers Squibb Uxbridge
Hybrid

Associate Director, Biostatistics

As a member of cross-functional development teams, you will contribute to trial design, protocol development, analysis planning, and regulatory submissions. The role involves authoring statistical analysis plans and clinical study reports, defending protocols at governance reviews, and providing statistical leadership on health authority requests. It requires 50% onsite presence in Uxbridge and offers the chance to support a specific asset indication.

Bristol Myers Squibb Uxbridge
Hybrid

Exec Director, Clinical Development (MD)

Leads clinical development strategy for multiple myeloma cell therapy programs, overseeing trial design, conduct, reporting and regulatory submissions. Represents products in governance committees, provides medical monitoring, and manages a team of direct reports while building external thought-leader relationships.

Gilead Sciences Uxbridge
Hybrid

Principal Scientist, Inflammation Research

Lead a team of scientists developing novel biologic therapies for autoimmune disease, overseeing in vitro and in vivo pharmacology studies for lead and early discovery programs. Collaborate across immunology, protein engineering, translational medicine and biomarkers to deliver data packages for progression to development, while mentoring staff and contributing to INDs and patents.

Gilead Sciences Oxford

Clinical Project Leader / Senior Project Leader - Biotech (Select EU countries)

Leads global clinical trial delivery for biotech clients, owning project plans, budgets, P&L, risk management and cross-functional team leadership. Acts as the primary client contact at study level, representing project leadership in bid pursuits and investigator meetings. Requires strong CRO background and therapeutic expertise in oncology plus a secondary area.

Parexel London
Remote