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 an…
Global Patient Access Enablement, Reporting & Insights Lead, Associate Director
Zurich, Zurich, Switzerland · On-site
$159k–$219k/yr
Senior+$2.5B raised
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 an…
Skills: Dashboard Development, Reporting Governance, Data Modeling, Real World Evidence, Project Management
Senior Consultant Generative AI & Agentic AI 60-100%
Bern, Bern, Switzerland · Hybrid
Senior
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$149k–$204k/yr
Full-time
bachelor degree, postgraduate degree
Posted 42d ago
~40 hrs/week
Responsibilities
Lead the design and implementation of Global Patient Access capabilities and operationalize Compassionate Use access programs. Coordinate cross-functionally with supply chain, medical, and legal teams to ensure compliant execution and performance reporting.
Requirements
Requires a degree in a relevant field with 3-8+ years of experience depending on the level of education, specifically in clinical research or early access programs. Must have 5+ years of project management experience and a strong understanding of global regulatory requirements and ICH GCP.
Full job description
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 of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
Location: While a primary location is identified for this role, qualified internal candidates located in Cambridge, MA, USA may also be considered, subject to business needs, role requirements, talent availability, and local legal requirements.
Compensation: The salary range displayed reflects the primary location associated with this posting. Compensation may vary for candidates considered in other locations. Where applicable, location-specific salary ranges and compensation information will be provided in accordance with local requirements.
OBJECTIVES/PURPOSE
Support the design, implementation, and continuous improvement of GPA capabilities, including processes, tools, and ways of working
Serve as a flexible, high-impact team member who can step into priority areas across GPA (e.g., operations, programs, compliance) to address gaps and drive execution.
Lead the transition and execution of Compassionate Use access programs, ensuring seamless end-to-end operationalization through cross-functional and NGO partnerships, including patient transition planning and execution
Deliver programs reporting and operational performance oversight (e.g., patient status tracking, transition progress, issue log, risks/escalations) for programs.
ACCOUNTABILITIES
Contribute to the design, implementation, and continuous improvement of GPA capabilities, including processes, tools, governance, and ways of working.
Lead the execution and optimization of Compassionate Use Access programs through coordination, tracking, and process improvement.
Coordinate cross-functionally with Supply Chain/Clinical Supply, PV/Safety, Quality, Medical, Legal/Compliance, vendors, and NGOs to ensure compliant, timely execution and rapid issue resolution.
Deliver Compassionate Use Access programs reporting and insights to support operational and strategic priorities
Own and maintain execution trackers (e.g., patient status, milestones, exceptions, issue log) and provide regular status updates to stakeholders and leadership.
Identify operational risks and bottlenecks early (e.g., country readiness, supply constraints, partner readiness), propose options, and drive decisions through to closure.
Develop practical solutions, templates, and frameworks that enable teams to operate more effectively.
Partner with functions such as Strategy & Operations, Compliance, Medical, and Vendors to drive aligned execution and adherence to global standards and ways of working.
Support operational execution across programs, including problem-solving, issue resolution, and coordination of activities.
Act as a flexible resource across Global Patient Access, stepping into high-priority areas or covering gaps to ensure continuity of delivery, as based on agreed prioritization.
EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:
Required
Education & Experience
PhD, PharmD with ~3+years; MS with ~5+ years; BS with ~8+ years experience or related experience in clinical research and/or early access program in the pharmaceutical industry or CRO
Experience in Patient Access, Global Medical Operations or related functions
5+ years of effective project management, clinical operations, Patient Access
Experience with digital tools leveraging digital platforms, data tools, and analytics solutions to support operational excellence, governance, and data‑driven decision‑making across global teams.
Good understanding of global regulatory and compliance requirements for patient access, clinical research, including but not limited to good knowledge of medical terminology, e-CRF, clinical data and ICH GCP
Experience working with clinical supply/supply chain, vendors and external organizations (including corporations, associations, non-governmental organizations, and academic institutions) relevant to the patient access field
Experience working within a complex, global organization and demonstrated ability to work across functions at all levels without minimal direct authority
Behavioral Competencies & Skills
Structured and detail‑oriented, with a strong focus on quality and accuracy.
Comfortable working through ambiguity and evolving priorities.
Preferred
Advanced degree in a health, life sciences, data, or technology‑related discipline (e.g., Pharmacy, Public Health, Health Informatics, Data Analytics).
ADDITIONAL INFORMATION
Percentage of travel: Requires approximately 10% travel, including overnight and international travel to other Takeda sites and meetings with external partners
Locations
Zurich, Switzerland
Base Salary Range:
CHF148,600.00 - CHF204,270.00
For information about our benefits, please click here.
We strive to transform lives. While the science we advance is constantly evolving, our core purpose is enduring. For more than two centuries, our values have guided us to do what’s right for patients and for society.
We know that changing lives requires us to do things differently. We start by listening to and addressing what really matters to patients, the people who love them, and those in the healthcare system who provide care. And that’s what inspires us all to be bold, push boundaries and set new standards that open up greater opportunities.
Read our community guidelines: https://takeda.info/communityguidelines
Offices: Tokyo, JP · 1 Takeda Parkway, Deerfield, Illinois 60015, US · 40 Landsdowne St, Cambridge, Massachusetts 02139, US · Avenida das Nações Unidas, 14.401, Torre Jequitibá - 10°, 11° e 12° andares, São Paulo, 04794-000, BR · 43 Old Oak Rd, Bellville, Western Cape 7550, ZA
How many Data & Analytics jobs are open in Zurich, Switzerland right now?
There are currently 527 open data & analytics positions in Zurich, Switzerland listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Data & Analytics roles in Zurich, Switzerland?
Companies currently hiring include Julius Baer, Google, ETH juniors, PwC, Amazon, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Data & Analytics jobs in Zurich, Switzerland?
Yes — 235 of the 527 open data & analytics positions offer remote or hybrid work (42 remote, 193 hybrid).
How do I apply for Data & Analytics jobs in Zurich, Switzerland?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.