PHC Partner

Taiwan, Taipei City, Taipei

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Objectives and Scope of Position:

  • Functional agonistically accelerate PHC and showcase PHC value within defined oncology ecosystems and beyond (e.g. pan-tumor and even pediatrics)

  • Is activated by other Roche PJPs/HSPs to prompt value of CGP and FMI solutions with advanced/academic engagement

  • Operationalize PHC experiments to establish CGP value and position FMI in clinical practice

  • Point of contact for PHC ecosystem activities for selected strategic stakeholders (eg , building partnerships: MTB development and institutionalization; RWD collection set-up and maintenance)

  • Primary point of contact for FMI CGP solution for a target group (e.g. TAEs outside defined oncology ecosystems), and accountable to collect insights and develop strategies with PJPs/HSPs and enabling teams

Primary Responsibilities and Accountabilities:

1. Accountable for FMI patient reports interpretation for selective physicians

2. Triggered by PJPs/HSPs to deliver advanced / educational conversation i.e. NGS/CGP platform technology and up-to-date MGTO relevant knowledge

3. Establish long-term, peer-to-peer relationships with TAEs particularly in which tumor types Roche is having and/or will have portfolio presence in near future

4. Connect PI(Pharma International)  Medical and selective strategic accounts to experience Global MTB

5. Facilitate in-hospital or cross-hospital MTB; act as molecular biologist to provide genomic information / knowledge for MGTO discussion

6. Support PJPs/HSPs to engage account stakeholder to establish MTB

7. Deliver pipeline/MGTO presentations to selective customers on request

8. Providing customer insights and work with PJPs/HSPs/ET to align strategic plans

9. Follow the compliance with all relevant Roche guidelines and policies

10. Selectively support ST and OneRoche CGP Squad initiates for more MTB/MGTO/data transfer science conversation if needed

Experience, Skills, Knowledge

Proficiency in English


  • Professional experience within the pharmaceutical industry desirable but not mandatory

  • Experience in the principles and techniques of data analysis, interpretation, and assessment of clinical relevance for the purpose of understanding and communicating FMI reports and clinical study results

  • Experience in delivery of scientific presentations

  • Relationships with TAEs and external professional, disease, and research organizations is strongly preferred

  • Proven experience in working with multidisciplinary teams an asset clear decision


  • Pharmaceutical/NGS scientific knowledge (including molecular biology and bioinformatics etc.)  and market characteristics

  • Key Opinion Leader identification/development and management

  • Pharma Regulatory and Access environment

  • Work in cross-functional teams

  • Relevant therapeutic area Local laws, regulations and Codes of Practice

  • Computer/digital literacy (MS office, Google, etc.)

  • Fluent national language knowledge, written and verbal


  • Has in-depth conceptual and practical knowledge in own specialized area and basic knowledge of related areas

  • Solves complex problems, and takes a new perspective using existing solutions

  • Works independently within guidelines and policies, receives minimal guidance

  • May lead moderate projects or participate in large project teams; may have accountability for on-going activities/objectives and local portfolios

  • Acts as a resource for colleagues with less experience and provides functional

  • Awareness of the Roche organization and key organizational drivers as well as the relevant processes, customers and products related to own discipline