Latest Therapeutics Jobs

Director, Clinical Pharmacology

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.

Relation Therapeutics London

Hybrid Permanent

Vice President - Oncology Clinical Development, Disease Area Head- Hematology

Leads end-to-end clinical development of hematology oncology assets from first-in-human studies through registrational trials, regulatory approval and launch. Provides portfolio oversight, chairs governance forums and scientific advisory boards, and line-manages Clinical Development Leads and Medical Directors within a global matrix team.

GSK Stevenage

Hybrid

Vice President - Oncology Clinical Development, Disease Area Head- Hematology

Leads end-to-end clinical development strategy for a hematology oncology portfolio, from first-in-human studies through registrational trials, regulatory approval and initial launch. Provides program oversight at governance forums, co-leads asset development with matrix partners, and line-manages Clinical Development Leads, Medical Directors and Clinical Scientists. Champions novel approaches such as AI/ML, innovative trial designs and real-world data.

GSK London

Hybrid

Vice President, Biologics Process Development

Leads Ipsen's global Biologics Process Development organisation, owning CMC drug substance strategy for toxins, monoclonal antibodies, ADCs and enzymes from candidate selection through launch and lifecycle. Manages process and analytical development teams, acts as CMC sponsor, and directs CDMO partnerships, tech transfer and regulatory submissions. Also serves as PharmDev/R&D site lead in Wrexham on the cross-divisional Site Leadership Team.

Ipsen Wrexham

Senior Regulatory Submission Project Manager

Leads global cross-functional teams to plan, coordinate and deliver regulatory submissions such as new marketing authorisations and new indications. Manages integrated submission timelines, scenario planning, risk mitigation and forecasting, working with Regulatory Affairs, Clinical, Quality and Manufacturing. Requires CTD/eCTD filing expertise and project management tools in a global matrix environment.

Ipsen London

Hybrid

Associate Director, Biostatistics

Leads the full statistical contribution to a clinical development programme, defining statistical strategy and methodology for trial design, analysis and regulatory submissions. Represents Biostatistics in interactions with FDA, EMA and PMDA, manages CRO/FSP outsourcing, and provides thought partnership on innovative study design and Go-No Go criteria. Two positions available across multiple therapeutic areas.

CSL Amsterdam, Netherlands US$212,000 – US$251,000 pa

Hybrid Permanent

Senior Medical Director, Global Clinical Program Lead - Immunoglobulins

The Senior Medical Director, Global Clinical Program Lead is responsible for the strategic leadership of the Clinical Development Team, ensuring the design and execution of clinical strategies for immunoglobulin medicines. Key responsibilities include leading cross-functional teams, maintaining alignment with stakeholders, and ensuring compliance with regulatory standards.

CSL Maidenhead

Medical Affairs - Industrial Placement (12 Months)

A 12-month industrial placement within an international Medical Affairs team, supporting the planning and execution of medical projects in assigned therapeutic areas. The role involves project management, monthly dashboard reporting, managing external agencies, monitoring budgets for medical education events and advisory boards, and liaising with cross-functional and external stakeholders.

Vertex Pharmaceuticals London

Hybrid Internship

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

Lead the development, qualification, validation and execution of complex cell-based immunoassays generating high-quality data for clinical trials across multiple therapeutic areas. Act as scientific point of contact within the Immuno-assays group, collaborating with multidisciplinary teams and external partners, and coaching junior laboratory staff.

Moderna Clinical Development

Hybrid Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

Provides scientific and hands-on oversight of ligand binding assay bioanalysis and immunogenicity testing for mRNA-LNP therapeutic programs, leading ADA and neutralizing antibody assay development, validation and clinical sample testing. Ensures GcLP compliance, reviews analytical data and supports regulatory submissions within cross-functional clinical development teams.

Moderna Clinical Development

Hybrid Permanent

CRA II - SCRA I - Midlands - FSP

Monitors and oversees clinical trial sites across the Midlands, handling site initiation, monitoring visits and closeouts while ensuring GCP compliance and patient safety. Also supports feasibility assessments, investigator recruitment, vendor coordination, SAE reporting and mentoring of junior team members within a global FSP team.

Fortrea Maidenhead

Senior Technical Specialist - Stem Cell

Acts as subject matter expert for stem cell culture technologies, leading development, optimisation and delivery of cellular systems for drug discovery. Manages multiple cell culture programmes, supplies high-quality cell batches for high-throughput screening, and troubleshoots assays while ensuring biological safety compliance. Collaborates with multidisciplinary teams and external partners across global sites.

IQVIA Cambridge

Associate Research Leader - Stem Cells

Leads stem cell-focused drug discovery projects, designing and optimising human iPSC-derived models, 2D/3D assays and disease models, and applying New Approach Methodologies to client programmes. Partners directly with pharmaceutical and biotech clients, presenting data and shaping project strategy, while mentoring colleagues and contributing to proposals and capability development.

IQVIA Cambridge

CRA II/SCRA , London (client-dedicated)

Conducts and oversees site monitoring visits, managing site initiation, monitoring and closeouts while ensuring patient safety, data integrity and GCP compliance. Supports feasibility assessments, investigator recruitment and vendor coordination, and mentors junior team members. Requires Phase I patient-study experience within a client-dedicated FSP team.

Fortrea Maidenhead

Scientist

Early-career scientist role in a Life Sciences team, generating therapeutic hypotheses by mining in-house genomic data with statistical methods to identify and triage drug targets. Also develops and optimises polygenic risk score tools for patient stratification, working with omic data using statistical and AI/ML approaches and communicating findings to internal and external stakeholders.

Genomics London

Hybrid Permanent