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Parexel

End-to-end clinical trials and regulatory consulting

Executive Director - HEOR Modeling

Strategy & Management ConsultingConfirmed live in the last 24 hours
Full-timeRemote in USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a scientific or technical discipline.
  • 15 or more years of general experience in the field.
  • 10 or more years of management experience.
  • Experience in the life sciences or consulting industries, including managing direct reports and directing teams and projects.
  • Fluent written and spoken English.

Responsibilities

  • Lead small and large project engagements, ensuring high-quality delivery, client satisfaction, appropriate scope, and effective issue and conflict resolution.
  • Monitor project profitability through project planning, budget management, revenue recognition, and collaboration with the assigned Project Financial Analyst.
  • Develop and implement business solutions that address client needs using HEOR expertise, industry best practices, and knowledge of key business drivers.
  • Act as a trusted advisor to clients, including senior and executive leaders, and provide technical and business consulting services across multiple disciplines.
  • Lead, coach, mentor, and develop direct reports and extended staff, including performance management, development planning, succession input, workload prioritization, and accountability for key metrics.
  • Identify and pursue new and repeat business opportunities, contribute to account planning, participate in scoping and proposal development, and deliver sales presentations and bid defenses.
  • Support strategy and decision-making for Parexel Access Consulting across HEOR, patient market access, and access analytics.
  • Stay current on artificial intelligence developments relevant to HEOR, including machine learning, natural language processing, data analytics, and predictive modeling, and apply them to innovative research and analytical methodologies.
  • Collaborate with data scientists, biostatisticians, health economists, Global Centers of Excellence, and other cross-functional partners to develop artificial intelligence-driven methods, tools, publications, and educational materials.
  • Represent Parexel through conferences, scientific symposiums, webinars, publications, regulatory and academic engagement, and strategic partnerships with key opinion leaders and influential organizations.
  • Plan budgets, strategy, and forecasts for the assigned service line or group, with accountability for revenue generation, client satisfaction, service delivery, and financial outcomes.
  • Follow required Business Operating Processes and complete established annual scorecard metrics and core job responsibilities.

Desired Qualifications

  • An advanced degree such as a Master of Science, PhD, or MD.
  • Experience developing and delivering HEOR consulting services.
  • Experience applying or advancing artificial intelligence-related methodologies in HEOR, including machine learning, natural language processing, data analytics, or predictive modeling.
  • Established industry visibility through conferences, scientific publications, external partnerships, or client relationships.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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