HEOR Project Manager - The Fountain Group

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 client of 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. 

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.

Required Skills & Qualifications:

• 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

Preferred Skills & Qualifications

• Understanding of Real World health outcomes research/observational research 
• Knowledge of pharma regulatory / HTA environment