HEOR Project Manager
2 months ago
Hello,
The Fountain Group is a national staffing firm and we are currently seeking a Project Manager Scientific III (HEOR/Pharma/Regulatory) for a prominent clientof ours. This position is located in Research Rahway, NJ (hybrid) Details for the position are as follows:
Job Description:
Details
- Pay for this position is 50.00 to 61.87 hourly depending on experience.
- This position is hybrid - 3 days onsite per week required.
- This position is a one-year contract with the possibility of extension or conversion to permanent.
- 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.
- Education: Bachelor's 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
- Understanding of Real World health outcomes research/observational research
- Knowledge of pharma regulatory / HTA environment
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