Clinical Science Lead — Global Trials & Real-World Evidence

Takeda Pharmaceutical; Zürich; Sur place; CHF 177 000 - 244 000; Plein temps

Résumé du poste

Takeda Pharmaceutical Co. in Zürich, Switzerland invites an experienced Director-level leader to shape scientific and operational strategy for clinical studies across Phase 3B, Phase 4, and real-world evidence initiatives.

You will drive study design, governance, and vendor oversight while leveraging digital and AI-enabled tools to strengthen planning, oversight, analytics, and decision-making. The role emphasizes quality, compliance, and business priorities across interventional and

Qualifications

• Advanced degree in scientific/clinical/epidemiologic/quantitative or health-related discipline.
• 10+ years of experience in clinical development, evidence generation, clinical research, or related disciplines involving interventional and non-interventional studies.
• Significant experience in clinical science, clinical development, study implementation, epidemiology, real-world evidence, or related biopharmaceutical functions.
• Strong experience authoring, reviewing, and approving clinical trial protocols and related study documentation.
• Experience leading global or multi-country clinical studies through implementation and publication.
• Extensive knowledge of interventional and non-interventional study designs, good clinical practice, applicable regulations, ethics, quality standards, and standard operating procedure-driven practices.
• Demonstrated ability to interpret complex clinical and safety data and communicate findings effectively to diverse audiences.
• Strong program leadership, stakeholder management, vendor oversight, decision-making, and team leadership skills, including experience using digital and artificial intelligence-enabled tools in a regulated environment.

Responsabilités

• Provide scientific and operational leadership for planning, implementation, oversight, execution, and reporting of clinical, real-world evidence, and externally sponsored studies.
• Lead study design and document development through creation, review, and approval of protocols, amendments, study concepts, and related materials.
• Ensure study quality and feasibility by aligning study designs and execution plans with evidence generation priorities and stakeholder needs.
• Manage study delivery and performance by overseeing timelines, enrollment, budgets, operational metrics, risks, and quality indicators.
• Interpret and communicate clinical findings by translating complex clinical and safety data into recommendations, reports, publications, and decision-support materials.
• Partner across functional teams to support compliant study governance, vendor oversight, contracting, reporting, and archiving activities.
• Lead vendor and external partnership management while maintaining budget stewardship across the assigned portfolio.
• Drive continuous improvement and innovation through the adoption of digital and AI-enabled tools that enhance evidence generation and study management.

Formation

Advanced degree in scientific/clinical/epidemiologic/quantitative or health-related discipline

Description du poste

Takeda Pharmaceutical Co. in Zürich, Switzerland invites an experienced Director-level leader to shape scientific and operational strategy for clinical studies across Phase 3B, Phase 4, and real-world evidence initiatives.

You will drive study design, governance, and vendor oversight while leveraging digital and AI-enabled tools to strengthen planning, oversight, analytics, and decision-making. The role emphasizes quality, compliance, and business priorities across interventional and