Senior MA Manager (Team Leader)
Veröffentlicht:
16 Mai 2024Pensum:
100%Vertrag:
Festanstellung- Arbeitsort:Zuchwil
POSITION SUMMARY: Briefly state the objective of this position. Why the job exists (2-3 sentence maximum)
l Lead MA team to d evelop medical strategy (both in-market products and pre-launch for product portfolio) with support from DAS Lead
l Lead team to develop data generation and dissemination plan based on strategy, 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 p rogress in relevant therapeutic areas & products/competitors and sharing with cross-functions etc.
l Ensure 100% high quality & compliance delivery of MA team KPIs
l Keep close communication and engagement with internal & external key stakeholders.
l Responsible for team management
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 team to develop 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.. E nhance the influence of China in AP/Global.
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 team to develop and deliver MA plan & KPIs with high quality & 100% compliance.
a) Data generation plan and execution including IEGP & clinical trial management.
i. Ensure the study is designed and operated in compliance with related SOP and other required regulations.
ii. Design and compose creative 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.
iii. Lead and drive the study progress/publication plan, review study report, carry out medical monitoring during the clinical study.
iv. MAO/CRO collaborations on study operation.
v. Collaboration with Statistician and Data Management team for SAP and data monitoring as required.
vi. Ensure the AEs in the study are reported as required.
b) determination of the theme & high-quality medical content of national activities and expert discussion, collaboration for medical educational activities
c) 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.
d) Expert review and provision of careful, thoughtful input into the promotional/educational materials and other project-based activity materials from a scientific viewpoint.
e) Provide TA or product related training/support to Marketing/Sales and other departments.
50%
3. Keep close communication and engagement with internal & external key stakeholders.
a) Lead 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.
b) Good academic engagement of national KOLs
20%
4. Responsible for team management
a) Establish and sustain trust and aspiration under healthy team cultures.
b) Keep reasonable turn-over rate within team
c) Manage budget plan of MA team
10%
Total
100%