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POSITION SUMMARY

Develop medical strategy and medical projects, including clinical study design & operation; determination of the theme & high-quality medical content of national activities and expert discussion, collaboration for medical educational activities; understanding recent progress in relevant therapeutic areas & products/competitors and sharing with cross-functions; communication and collaboration with internal and external customers; expert review and providing scientific input into the promotional/educational/project-based materials; providing TA or product related training/support.

RESPONSIBILITIES may include but no limited to

• Development and execution of medical strategy:

• Responsible for productive discussion with internal cross-functions including Global/AP, medical insights collection with key national external stakeholders including KOLs etc..
• Responsible for exhaustive collection of information regarding the latest progress in therapeutic areas/products/competitors, existing knowledge gaps, scientific evidence gaps and clinical practice gaps.
• Responsible for authoring the Medical Strategy after collection of input and insights from a wide cross-section of internal and external stakeholders.
• Responsible for directing medical strategy and developing medical projects.

• Clinical study management

• Ensure the study is designed and operated in compliance with related SOP and other required regulations.
• Design and compose clinical study protocols as required; submit concept/protocol for internal review and approval; manage the study budget and phasing; ensure the registration of the study online as required; present at investigator meeting if necessary.
• Set plan for CSR and publication; review study report; carry out medical monitoring during the clinical study.
• MAO/CRO collaborations on study operation.
• Collaborate with Statistician and Data Management team for SAP and data monitoring as required.
• Ensure the AEs in the study are reported as required.

• Determine the theme and high-quality medical content of national activities including advisory board and expert discussion; Contribute to the theme of medical educational activities and materials. Closely work with ME/MSL team when necessary.

• Understand the recent progress in literature/congress in relevant therapeutic areas and products/competitors, HCP perceptions; Generate insights from the above resources, then integrate and share with cross-functional team.

• Establish good communication and cooperation with internal and external customers, including Global and Regional (AP) MAF, R&D (CD, RA, CDTL et al.), ME, MSL, MKT, Sales, PR, BD, Strategic MKT, MKT Access, CRO etc.

• Expert review and provision of careful, thoughtful input into the promotional/educational materials and other project-based activity materials from a scientific viewpoint.

• Provide TA or product related training/support to Marketing/Sales and other departments.

COMPETENCIES/SKILLS/REQUIREMENTS

• 2-3 years clinical working experience on relevant therapeutic area/or 1-2 years working experience on pharmaceutical industry is preferred.

• Thorough understanding and command of GCP, HCC.
• Good command of English, fluent at reading, writing, speaking and listening.
• Thorough understanding and command of product and relevant therapeutic area knowledge.
• Agile strategic thinking with the development of medical strategy/projects based on unmet needs and aligned with cross-functions.
• Identify data gaps, and collaborate with internal/external stakeholders for study design/operation/publication to meet the gap.
• Implement scientific communication with evidence-based medical content/information via multiple ways.
• Establish trust relationship and collaboration with cross functions, with aligned strategy/responsibilities, providing valued scientific suggestions for the high-quality output.
• Develop action plan for insight collection and KOL engagement based on medical strategy, establish and maintain collaboration with external customers.

OTHERS

• Domestic and International travels are required.

• 试用期内按照公司要求完成入职培训、合规培训及考核并达到相关要求（该等条件和要求属于员工应满足的录用条件，如未能按照公司要求完成相关测试、培训并满足考核，将视为试用期内不符合录用条件。）

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