Latest Gene Therapies Jobs

Director, Regional Ecosystem Lead (Northern Europe & UK)

Leads CSL's engagement in the Northern Europe and UK biotech innovation ecosystems, building strategic relationships with academia, biotech firms, and investors to identify and drive partnership opportunities. Acts as a senior deal team member, sources external innovation aligned with therapeutic area priorities, and represents CSL at industry events and boards. Requires deep regional network expertise and collaboration with global R&D and business development teams to strengthen the company’s innovation pipeline.

CSL

Hybrid Permanent

Specialist, R&D Contracts & Business Operations

This role supports R&D contract management and business operations within a global biopharmaceutical organization. The specialist will handle end-to-end contract processes including drafting agreements, managing purchase orders, ensuring compliance, and maintaining accurate records. Collaboration with cross-functional teams is essential to track obligations, ensure timely approvals, and promote operational efficiency in a hybrid working environment.

CSL

Hybrid Permanent

Clinical Development Medical Director - Neuromuscular

Leads global clinical development programs in neuroscience, with a focus on neuromuscular or related disorders. Provides medical and scientific leadership across trial design, regulatory submissions, and data interpretation. Engages with regulatory bodies and key opinion leaders to shape clinical strategy and advance innovative therapies.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Clinical Development Medical Director - Neuromuscular

Leads global clinical development programs in neuroscience, with a focus on neuromuscular or related disorders. Provides medical and scientific leadership across trial design, regulatory submissions, data interpretation, and external engagement. Works cross-functionally to drive innovative therapies from concept to approval, with emphasis on gene therapy and complex clinical data.

Novartis Ireland €90,300 – €167,700 pa

Hybrid Permanent

Principal Scientist, Bioanalytical & Molecular Assays

This role involves leading the development and validation of advanced molecular assays—including RT-qPCR, dPCR, and NGS-based methods—for clinical biomarker programs at Moderna. The scientist will drive end-to-end assay lifecycle management, ensure compliance with GCLP and regulatory standards, and collaborate across multidisciplinary teams to generate high-quality genomic data. A key focus is integrating genomics, bioinformatics, and clinical insights to support drug development and inform future pipeline strategies.

Moderna

Hybrid Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assays (LBA) in support of Moderna’s mRNA-LNP therapeutic programs. The Principal Scientist will oversee regulated bioanalytical activities including assay development, validation, and sample analysis, ensuring compliance with GcLP, GLP, and GCP standards. The position plays a key role in clinical development by generating high-quality data to inform regulatory submissions and advance innovative medicines, with opportunities to engage in AI-enabled and digital analytical approaches.

Moderna

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic area opportunities, from Phase 2 through marketed drugs. Responsibilities include engaging with Key Opinion Leaders, driving due diligence, and shaping the portfolio through high-impact partnerships.

CSL United States US$263,000 – US$328,000 pa

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

Lead the strategic sourcing and evaluation of late-stage therapeutic assets in Immunology, Hematology, or related areas, from Phase 2 through marketed drugs. Drive cross-functional due diligence, engage with key opinion leaders and clinical networks, and shape portfolio strategy through high-impact partnerships and transactions. Operate within a global biotech ecosystem with strong collaboration across R&D, BD, and regulatory functions.

CSL US$263,000 – US$328,000 pa

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation into portfolio planning. The position requires deep clinical expertise, a proven track record in deal-making, and strong collaboration with cross-functional teams.

CSL US$263,000 – US$328,000 pa

Hybrid Permanent

Senior Clinical Trial Case Manager

Manages clinical trial case management activities, ensuring compliance with international and national regulations including GxP and pharmacovigilance standards. Oversees safety reporting, vendor performance, and case processing for serious adverse events, while acting as a key liaison for inspections and audits. Provides training, supports database enhancements, and ensures accurate coding and consistency in safety data analysis.

CSL

Vaccines Safety Sciences Lead

Leads and manages pharmacovigilance functions, ensuring compliance with global regulatory standards and GxP guidelines. Oversees signal detection, safety data analysis, and regulatory documentation while providing strategic direction for process improvements and inspection readiness. Acts as a subject matter expert in safety sciences, leading teams and contributing to drug development and post-marketing safety initiatives.

CSL

Hybrid Permanent

Vaccines Safety Sciences Lead

Leads and manages pharmacovigilance and safety sciences functions, ensuring compliance with global regulatory standards and GxP guidelines. Oversees signal detection, safety data analysis, and regulatory documentation such as the PSMF, while driving process improvements and supporting PV inspections. Acts as a strategic expert in implementing safety systems and translating business requirements into technical solutions for global teams.

CSL

Hybrid Permanent

Director, Search & Evaluation Early TA Lead (CVR and Haem)

Leads strategic sourcing and evaluation of early-stage innovation in Hematology and Cardiovascular/Renal therapeutic areas, identifying preclinical to Phase 1 assets. Drives external partnership strategies, coordinates cross-functional due diligence across scientific and clinical domains, and supports deal execution. Embedded within therapeutic leadership teams to align external opportunities with portfolio strategy.

CSL

On-site Permanent

Director, Search & Evaluation Early TA Lead (CVR and Haem)

Leads strategic sourcing and evaluation of early-stage external innovation in Hematology or Cardiovascular/Renal therapeutic areas. Identifies and advances preclinical to Phase 1 assets, drives due diligence, and shapes partnering strategies within cross-functional teams. Represents the therapeutic area externally, building relationships with biotech, academia, and investors to strengthen the innovation pipeline.

CSL

On-site Permanent

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety across the product lifecycle, focusing on clinical safety evaluation, signal detection, and risk management. Oversees production of key pharmacovigilance documents and ensures compliance with regulatory standards. Acts as safety representative in cross-functional teams and drives safety specifications and risk mitigation plans.

CSL