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Associate Principal, Regulatory Science & Strategy

Aplica ya
Mapa de ubicación: Falls Church, Virginia, United States Full time R1311083

Descripción del trabajo

Job Overview

As an Associate Principal within the IQVIA Regulatory Science and Strategy Practice, you will bring scientific expertise, relationship-building skills, and program management expertise to help IQVIA win and execute on RWE regulatory strategy business. Our projects include advisory consulting on regulatory strategy and rationalizing use of real word evidence for regulatory decision making. These projects can be stand alone or a component of a large project for a life sciences client. The main focus of the Associate Principal role is to deliver outstanding program and study leadership, while building trusted relationships with all external and internal stakeholders.

Responsibilities

  • Develop and deliver insightful, value-added strategies that address complex client issues. Create and elevate new opportunities through the identification of value-added follow-on work and identify new revenue opportunities with existing and new client organizations.
  • Act as principal owner of program engagements, in some cases with mentoring from senior staff. Ultimate responsibility for client satisfaction and delivering high levels of quality. In many cases, this will require application of scientific / healthcare expertise as well as leadership acumen.
  • Allocate direction, advice, and intellectual leadership to clients and delivery teams. This includes working with other IQVIA teams to ensure the larger program objectives are achieved across multi-stakeholder collaborations.
  • Provide high level input and ensure development of key reports and presentations that are essential to program delivery.
  • Contribute on or lead thought leadership and internal initiatives.
  • Remain current on latest regulatory trends and clients in order to anticipate and identify new business challenges and issues with assigned opportunities.
  • Mentor, coach, and share subject matter expertise with others to help develop individuals and capabilities delivering world-class solutions for clients.


Qualifications

Our ideal candidate will have

  • US location (work from home), preference for East Coast US with ability to travel to Washington DC.
  • A Bachelor's degree and an advanced degree related to health care (for example, epidemiology, health economics, health outcomes, health administration, pharmacy, medical doctor). Experience may substitute for advanced degree.
  • In addition to advanced degree, 3-7 years (depending on advanced degree and hiring level) relevant experience in regulatory programs and studies.
  • Strong project management, program management, and leadership skills; particularly multi-stakeholder leadership.
  • Acumen with real-world data, real-world evidence, clinical outcomes assessments, and study design. Should also have broad understanding of the pharmaceutical and medical device industries.
  • Able to work in environment with ambiguity and help develop the structure as the team grows.
  • Learning agility and willingness to continuously improve how IQVIA structure and deliver successful regulatory science-related initiatives.
  • Some flexibility to support client-facing business travel (10-25%).

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

As the COVID-19 virus continues to evolve, IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status

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