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

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

Qualification and Experience
Education/Qualifications

• Medical or PhD/PharmD degrees preferred. Other graduate health science degrees, or equivalent with strong proven therapeutic area experience considered.
• 1-2 years working experience with Medical, sales & Marketing in Pharmaceutical company desirable but not mandatory, OR as medical doctor in hospital
• Experience in therapeutic area strongly preferred
• Experience in delivery of scientific presentations preferred
• Relationships with TAEs, other thought leaders, and external professional, disease, and research organizations is strongly preferred
• Proven experience in working with multidisciplinary teams an asset

Job Required Competencies

• Local laws, regulations and Codes of Practice
• Computer literate (MS office, Google, etc.)
• English knowledge highly desirable
• Knowledge in data analysis and statistics for purpose of understanding clinical study results
• High ethical standards
• Strategic thinking
• Collaboration skills
• Roche/GNE leadership competencies
• Analytical Skills
• Results orientation
• Relationship skills
• Communication, interpersonal and networking skills
• Presentation skills