Specific assignments may include (but are not limited to):
Collate, clean, validate and integrate data on Health Technology Assessment (HTA) Submission Tracking from multiple sources
Summarize HTA Submission Tracking information for executive and detailed reporting (slides, Qlik Sense dashboard and define requirements for IT to develop a customized report in an existing web-app)
Compare internal HTA data and other external resources/repositories
Analyzing and cleaning data related to HTA planning needs from a customized web app, in collaboration with multiple stakeholders (including monitoring of related ongoing clinical trials and regulatory filing opportunities imported from other internal sources)
Support to automate data collection for HTA Submissions and for some scoping activities in relation to EU HTA Regulation
Support with development activities for the internal HTA tracking web app (business requirements definition and design review only, no design and coding)
Lead data governance and generic data quality initiatives
Project management support in defining the work plan and tracking HTA related projects with multiple stakeholders
Ad hoc HTA analysis (business driven)
Support to describe, review and adjust internal process related to HTA.
Support to evaluate impact of evolving HTA regulations on internal process.
Develop and review training material.
Quals--
Required Skills & Qualifications
Education: Bachelors Degree in scientific, business, ore related health care area. Master's degree Preferred.
4-5 years working experience, preferably related to the pharma regulatory / HTA / market access environment
Data analysis capability, comfortable with data and big data management
Good knowledge of MS Office package
Process-oriented, accurate and detailed
Flexible and open minded
Excellent written, verbal and interpersonal communication skills
Ability to lead and manage working teams without formal reporting structure
Ability to collaborate across functional areas and geographic boundaries
Strong project management and prioritization skills with demonstrated ability to deliver on operational objectives for complex projects, portfolio planning and project management
Highly motivated, able to work independently and collaboratively, raising issues with recommendations for solutions
Hybrid - 3 days a week in onsite required
Preferred Skills & Qualifications
Understanding of Real World health outcomes research/observational research
Knowledge of pharma regulatory / HTA environment •
Last updated on Nov 28, 2023