Biotechnology Jobs

20 jobs for “Protein Engineer”

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Medical Evaluator - Global Case Management

2 days ago

CSL Haywards Heath

Oversees vendor delivery of medical evaluations for individual case safety reports, applying medical and scientific judgment on causality, expectedness and seriousness. Trains Medical Evaluators, sets assessment frameworks and drives process improvements across Global Safety and Pharmacovigilance. Requires deep pharmacovigilance knowledge and cross-functional stakeholder work.

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Associate Director, Biostatistics

2 days ago

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

Leads the full scope of statistical contribution to a clinical development programme, defining statistical strategy and methodologies for trial design, analysis and regulatory submissions. Represents Biostatistics in interactions with authorities such as FDA, EMA and PMDA, and manages outsourcing or internal statistical programmers. Two positions support multiple therapeutic areas.

Hybrid
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Associate Director, Biostatistics

2 days ago

CSL Opfikon, Switzerland US$212,000 – US$251,000 pa

Leads the full statistical contribution to a clinical development programme, defining statistical strategy for trial design, analysis and regulatory submissions, and representing Biostatistics in interactions with the FDA, EMA and PMDA. Also manages outsourcing to CROs and internal statistical programmers, and supports departmental improvement initiatives.

Hybrid
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Director, Search & Evaluation Early TA Lead (Haem)

2 months ago

CSL Maidenhead

Leads strategic sourcing and evaluation of external innovation opportunities in Haematology, identifying preclinical to Phase 1 assets and shaping early partnering strategies. Sits on the Therapeutic Area Leadership Team, co-leads New Product Opportunity reviews, drives cross-functional due diligence and works with Business Development on deal execution. Hybrid, three days a week at an R&D hub site.

Hybrid
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Director, Search & Evaluation Early TA Lead (Haem)

2 months ago

CSL Opfikon, Switzerland

Leads strategic sourcing and evaluation of external innovation opportunities in Haematology, identifying preclinical to Phase 1 assets and shaping early partnering strategies. Sits on the Therapeutic Area Leadership Team, co-leads New Product Opportunity reviews, drives cross-functional due diligence, and works with Business Development on deal execution. Hybrid, three days a week at an R&D hub site.

Hybrid
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Senior Director, Search & Evaluation Late TA Lead, Immunology

2 months ago

CSL Opfikon, Switzerland

Leads strategic sourcing and evaluation of late-stage external clinical assets in Immunology, from Phase 2 through marketed drugs. Sits on the Therapy Area Leadership Team, co-leads New Product Opportunity reviews, engages external KOLs and investigators, and drives cross-functional due diligence with BD to close deals.

Hybrid
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Senior Director, Search & Evaluation Late TA Lead, Immunology

2 months ago

CSL Maidenhead

Leads strategic sourcing and evaluation of late-stage external clinical assets in Immunology, from Phase 2 through marketed drugs, as the senior S&E leader within the Therapy Area Leadership Team. Drives proactive sourcing, cross-functional due diligence, and KOL engagement, partnering with BD to advance high-priority opportunities through negotiation and deal close.

Hybrid
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Senior Medical Director, Global Clinical Program Lead - Immunoglobulins

5 days ago

CSL Maidenhead

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.

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Senior Medical Director, Global Clinical Program Lead - Immunoglobulins

5 days ago

CSL Opfikon, Switzerland

The Senior Medical Director, Global Clinical Program Lead is responsible for the strategic leadership of clinical development programs, including team leadership, clinical oversight, and document authorship. The role involves cross-functional collaboration, regulatory interactions, and ensuring high scientific standards.

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