Job description

Requirements

  • Entry level
  • No Education
  • Salary to negotiate
  • Beijing

Description

Responsible for:
• Interacting with HCPs to understand their views, preferences and interests, in the assigned therapeutic area, and where Roche / GNE can partner with them to meet their needs where aligned with our strategies
• Providing medical expertise to customers, and customer insights to internal product teams
• Responding to unsolicited, product related questions from physicians in accordance to local laws, regulations and codes and Roche/GNE SOPs
• Serving as the scientific bridge and point of contact with the investigator for IISs, and supporting Roche/GNE sponsored study planning and execution including enhancing the site’s performance and quality
• Understanding and acting in line with legal, regulatory and company standards and codes of practice
• Inform Local Safety Responsible of safety issues according to Roche/GNE safety SOPs; and provide scientific support and follow-up on product safety issues
Key Activities:
1) Strategic partnership
• Interact with HCPs to understand their views, preferences and interests and where Roche / GNE 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 national advisory boards
• Acquire physician perspectives on competitive compounds / clinical studies
• Provide support to speakers on the development of materials
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2) Data Generation
• Receive IISs, championing the review of IISs within the company, and following-up with investigators, in accordance to all local laws and regulations
• 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 questions from HCPs in accordance to local laws, regulations and codes and Roche/GNE SOPs, facilitate their needs of up to date scientific data, including but not limited to publications of clinical trials, guidelines
• Work with CMM on the affiliate knowledge exchange strategy and execution, including preparation of presentations and scientific papers in their therapeutic area
4) Others
• Provide scientific support to Market Access colleagues for value dossier preparation
• Provide therapeutic and scientific training support to internal staff
• Provide information on site and investigator capabilities
• Deliver pipeline presentations to customers on request

About the company

Roche is a Swiss global health-care company that operates worldwide under two divisions: Pharmaceuticals and Diagnostics. Its holding company, Roche Holding AG, has bearer shares listed on the SIX Swiss Exchange.

The company headquarters are located in Basel and the company has many pharmaceutical and diagnostic sites around the world – including: Tucson, AZ; Pleasanton, CA; Vacaville, California, Oceanside, California, Branchburg, NJ; Indianapolis, Indiana; Florence, South Carolina; and Ponce, Puerto Rico in the US; Welwyn Garden City and Burgess Hill in the UK; Clarecastle in Ireland; Mannheim and Penzberg in Germany; Mississauga and Laval in Canada; Shanghai in China; Mumbai & Hyderabad in India; São Paulo and Rio de Janeiro, Brazil; Segrate, Milan in Italy; Johannesburg in South Africa; Karachi, Islamabad and Lahore in Pakistan. There are 26 manufacturing sites worldwide.

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