Associate Director, JCA Dossier Content (EU HTA)

The Associate Director, Joint Clinical Assessment (JCA) Dossier Content is a role within the Global Medical & Value Capabilities (GMVC) EUCAN & EEMEA Hub, responsible for developing and writing product specific JCA Dossiers in accordance with the requirements of the EU Regulation on Health Technology Assessment (HTAR).

Actively engage with key stakeholders to facilitate the creation and writing of product specific JCA Dossiers

Develop a clear understanding of the JCA Dossier template and associated content requirements as well as the implementation/submission procedures

Represents GMVC in the product specific regional JCA Dossier generation teams

Responsible to assure incorporation of appropriate and relevant content into the JCA Dossier working with cross-functional content experts

Works closely with Market Access, HTA statistics, regional Medical Affairs, Regulatory and the Global Value & Implementation (V&I) team to align dossier content with the value strategy

Aligns with countries on JCA Dossier content

All core activities have a Regional scope and impact. The Associate Director, JCA Dossier Content reports into the GMVC EUCAN & EEMEA Hub and will work closely with other key functions at the Local, Regional and Global level involved in strategy and content for the JCA Dossier.

Key Responsibilities Include, But Not Limited To:

Lead the writing of product specific JCA Dossiers in line with the overall product value strategy

Is responsible for the timely development of the required sections of the JCA Dossier template

Works closely with the EU HTA Dossier Lead in Market Access to assure timely execution of tasks

Actively provides input into strategic options related to dossier content

Works with the relevant functions to assure availability of content in a timely manner and a format which can be easily translated into dossier content