Medical Scientific Liaison
Taipei,Taipei City,Taiwan,
  • Job facts
  • Primary Responsibilities and Accountabilities

    1. Scientific partnership

  • Interacting with HCPs to understand their views, preferences and interests, in the assigned therapeutic area, and where Roche can partner with them to meet their needs where aligned with our strategies
  • Help profile physician practices, needs, preferences and views of new data
  • Determine physician interest in ongoing research and educational events
  • Participate / support the CMMs in the execution of regional advisory boards
  • Acquire physician perspectives on competitive compounds / clinical studies
  • Provide support to speakers on the development of materials
  • 2. Data Generation

  • Serving as the scientific bridge and point of contact with the investigator for ISTs
  • Receiving ISTs, championing the review of ISTs within the company, and following-up with investigators, in accordance to all local laws and regulations
  • Supporting Roche sponsored study planning and execution including enhancing the site’s performance and quality
  • Support site feasibility assessments, site development plan, recruitment, retention of patients enrolled in trials and enhancement of site management
  • Of Phase I-IIIa clinical studies under the direction of PD
  • Of Phase IIIb-IV Medical Affairs clinical studies in collaboration with Clinical Operations
  • 3. Knowledge exchange

  • Respond to unsolicited, product related questions from HCPs in accordance to local laws, regulations and codes and Roche SOPs, facilitate their needs of up to date scientific data, including but not limited to publications of clinical trials, guidelines, by ensuring they have the best quality available information they require
  • Work with CMM on the affiliate knowledge exchange strategy and execution, including preparation of presentations and scientific papers in their therapeutic area
  • 4. Others

  • Providing medical expertise to customers, and customer insights to internal product teams
  • With the CMM, providing scientific support to Market Access colleagues during discussions with payers to provide the scientific information to support payers in their decisions on government or hospital formulary / guidelines / protocols, etc.
  • With the CMM, provide therapeutic and scientific training support to internal staff
  • MSLs with focus on clinical trial activities may also support synopsis, protocol and CRF development
  • If applicable MSLs can provide information on site and investigator capabilities for gRED and pRED
  • Deliver pipeline presentations to customers on request
  • Understanding and acting in line with legal, regulatory and company standards and codes of practice (such as Roche Code of Conduct and any other directives, SOPs and guidelines)
  • Inform Local Safety Responsible of safety issues according to Roche safety SOPs; and provide scientific support and follow-
  • up on product safety issues

  • Who we are At Roche, 94,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-
  • focused healthcare groups. Our success is built on innovation, curiosity and diversity.

    Roche is an equal opportunity employer.

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