Director, Market Access, Health Technology Assessment Ops – Hematology (EU) at BeiGene

Basel, Basel-City, Switzerland -

Full Time

Start Date

Immediate

Expiry Date

12 Mar, 26

Salary

0.0

Posted On

12 Dec, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Market Access, Health Technology Assessment, Project Management, Cross-Functional Leadership, Evidence Generation, Regulatory Affairs, Oncology Experience, Interpersonal Skills, Communication Skills, Scientific Literacy, Medical Literacy, Data Analysis, Vendor Management, Continuous Improvement, Team Collaboration, Organizational Capabilities

Industry

Biotechnology Research

Description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: We are hiring an experienced EU HTA Coordination Lead to manage all operational activities related to the EU HTA Joint Clinical Assessment (JCA) and Joint Scientific Consultation (JSC) processes for assigned products. In this role, you will serve as the cross-functional coordinator responsible for ensuring timely, high-quality execution of all JCA and JSC procedural steps in alignment with the GVAP Portfolio Lead, who retains accountability for JCA strategy, JCA dossier, and JSC briefing book development. You will coordinate global, regional, and country contributors; manage project timelines; ensure consistent evidence inputs; lead meeting operations; and support submissions via the EU HTA IT platform. You will also facilitate internal alignment, vendor management, and collaboration with the EU HTA Coordination Group during JCA/JSC interactions. As EU HTA introduces new requirements and expectations, you will help shape internal operational processes, embed learnings, and build organizational capability in this evolving environment. Essential Functions of the Job: JCA Dossier Coordination & Operations Closely collaborate with the GVAP Portfolio Lead to drive the development of JCA dossier strategy and final JCA dossier delivery with cross functional teams team (incl. access, regulatory, HEOR, statistics, medical, clinical). Lead day-to-day operations for the JCA dossier team: SharePoint management, meeting scheduling, agenda drafting, minute-taking, and action tracking. Coordinate cross-functional inputs to ensure timely contribution to JCA strategy and dossier components. Work closely with HEOR to incorporate PICO simulation, consolidation, and feasibility assessments into JCA planning. Oversee evidence retrieval activities and ensure outputs are integrated into the dossier with the JCA writer. Coordinate epidemiology data collection across EEA markets and ensure alignment with Commercial/Forecasting. Coordinate cross functional LT and EU HTA governance board, GPT review of JCA strategy and JCA dossier. Manage dossier uploads and submissions via the EU HTA IT platform and support procedural interactions with EU HTA Coordination Group. JSC Dossier Coordination & Operations Support the EU HTA Strategy & Operations lead and GVAP portfolio lead in internal horizon scanning and assessing feasibility for initiating a JSC. In alignment with the GVAP portfolio lead, coordinate JSC operational activities incl. collection of cross functional input, request form submission, briefing book development, briefing book review, meeting scheduling, and documentation tracking. Engage SMEs and cross-functional teams to ensure readiness and consistent evidence positions. Project Management & Cross-Functional Leadership & Communication Develop and maintain comprehensive project timelines for all JCA and JSC activities. Ensure alignment of EU HTA JCA and JSC timelines with regulatory milestones (e.g., MAA), in partnership with the GVAP portfolio lead and regulatory affairs, incl. regulatory scenario planning, final assessment scope received, changes to indication etc. Ensure close collaboration and alignment with HEOR on PICO simulation, SLR, ITC timeline, information retrieval process, study list development. Ensure timely delivery of cross-functional contributions and maintain strong version control and documentation quality. Identify key risks early, propose mitigation strategies, and ensure procedural readiness at all stages. Internal Expertise Building & Continuous Improvement Drive continuous improvement by integrating lessons learned and optimizing internal workflows, templates, and operational standards. Support development of training materials and tools to enhance EU HTA readiness across global, regional, and affiliate teams. Promote knowledge management and consistent dissemination of best practices across the organization. Supervisory Responsibilities: No direct line management responsibilities. Extensive collaboration across functions, global, regional, country teams, and external partners/vendors. Education Required: Master’s degree required. Advanced degree (PharmD, MD, PhD) in a scientific, medical, or health economics discipline preferred. Computer Skills: Efficient in Microsoft Word, Excel, MS Project, MS PowerPoint and Outlook Other Qualifications: Masters degree with minimum 7+ years of experience in market access, evidence generation, or regulatory affairs within the pharmaceutical/biotech industry. Or 5+ years of experience with PharmD, MD, PhD. Proven experience leading cross-functional projects and driving alignment across diverse stakeholders. Strong project management and organizational capabilities with the ability to orchestrate complex, multi-stakeholder deliverables. Oncology experience strongly preferred. Excellent interpersonal and communication skills with the ability to prepare clear, concise, senior-ready documentation. Strong scientific & medical literacy with the ability to interpret clinical, epidemiological, and evidence-based data. Solid understanding of EU HTA Regulation (EU 2021/2282), JCA dossier templates, JSC processes, and Implementing Acts. Experience working with third-party vendors to deliver high-quality outputs. Ability to work independently, handle multiple priorities, and operate effectively in a fast-paced, evolving environment. Fluency in English (written and verbal). Travel: Limited travel may be required, up to 10% Global Competencies When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world. Fosters Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data Analysis Financial Excellence Communicates with Clarity We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. BeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 11,000 colleagues spans six continents. To learn more about BeOne, please visit www.beonemedicines.com and follow us on LinkedIn, X (formerly known as Twitter), Facebook and Instagram. For more information, please visit the link to explore job opportunities in China Mainland. China Mainland Job Posting At BeOne, how we work is just as important as the work we do. Below are our Values that determine the decisions we make and how we do things. Patients First Driving Excellence Bold Ingenuity Collaborative Spirit

Responsibilities

The Director will manage all operational activities related to the EU HTA Joint Clinical Assessment and Joint Scientific Consultation processes for assigned products. This includes coordinating cross-functional teams, managing project timelines, and ensuring high-quality execution of procedural steps.