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By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
About Reboot Monkey Reboot Monkey is a global datacenter services provider headquartered in Haarlem, Netherlands, operating 24 green-powered facilities across 6 continents . We deliver colocation, IP transit, smart hands, remote hands, and managed datacenter services to
About Reboot Monkey Reboot Monkey is a global datacenter services provider headquartered in Haarlem, Netherlands, operating 24 green-powered facilities across 6 continents . We deliver colocation, IP transit, smart hands, remote hands, and managed datacenter services to
Global Product Leader Some roles exist to manage processes. This one exists to make consequential decisions about medicines that matter to patients with serious diseases — and to ensure those decisions are made well, at pace, and
Patients depend on a continuous, compliant supply of medicines reaching the markets that need them. This role sits at the point where science, manufacturing, and regulation meet — translating CMC data into the submissions, change controls, and
Position Summary The Senior Director, Head of Medical Evidence reports into the Vice President, Head of Disease Areas and coordinates with Medical Affairs and cross-functional stakeholders to lead the Integrated Evidence Generation Plans (IEGP) for all
Role Overview The Senior Director of Market Access for Inline Assets will be responsible for shaping and implementing market access strategies for CSL Behring inline assets. This role is accountable for maximizing the asset total life
Role Overview: The Senior Director of Market Access for Inline Assets will be responsible for shaping and implementing market access strategies for CSL Behring inline assets. This role is accountable for maximizing the asset total life
What you will do Drive S&CM Process Governance & Maturity in the market: Drive focus on building S&CM process, capability, tools & data by setting ambitions linked to market needs, agreed action plan & milestone review. Provide
The Director Non-Clinical Due Diligence & External Evaluations provides scientific leadership for nonclinical due diligence supporting CSL’s in‑licensing, acquisitions, and strategic collaborations. The role ensures integrated, objective, and decision‑relevant evaluations of nonclinical pharmacology, PK/QSP, and toxicology
The Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. Manages a team of programmers supporting clinical trial and
Are you passionate about project portfolio management, data-driven decision-making, and enabling successful project execution? As a PMO Specialist, you will play a key role in ensuring transparency, governance, and operational excellence across our global project portfolio. Working closely
Role Overview: The Senior Director of Market Access for Inline Assets will be responsible for shaping and implementing market access strategies for CSL Behring inline assets. This role is accountable for maximizing the asset total life
CSLs R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means