HEOR Project Manager

4 weeks ago


Rahway, United States The Fountain Group Full time

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.
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

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