(Associate) MA Manager - Lung Cancer

POSITION SUMMARY : Briefly state the objective of this position.

Why the job exists (2-3 sentence maximum)

Develop medical strategy and medical projects, including clinical study design & operation; d etermination of the theme & high-quality medical content of national activities and expert discussion , collaboration for medical educational activities; u nderstanding 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.

PRINCIPAL RESPONSIBILITIES may include but no limited to:

Define major accountabilities and/or activities.

List most complex or difficult parts of job first and indicate percentage of time required to perform each task.

% OF TIME

1.

Lead development and execution of medical strategy:

1) Responsible for productive discussion with internal cross-functions including Global/AP, medical insights collection with key national external stakeholders including KOLs etc..

2) 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.

3) Responsible for authoring the Medical Strategy after collection of input and insights from a wide cross-section of internal and external stakeholders.

4) Responsible for directing medical strategy and developing medical projects.

20%

2.

Lead clinical study management

1) Ensure the study is designed and operated in compliance with related SOP and other required regulations.

2) 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.

3) Set up plan for CSR and publication; review study report; carry out medical monitoring during the clinical study.

4) MAO/CRO collaborations on study operation.

5) Collaborate with Statistician and Data Management team for SAP and data monitoring as required.

6) Ensure the AEs in the study are reported as required.

20%

3.

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.

10%

4.

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.

10%

5.

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, M...