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Parexel

End-to-end clinical trials and regulatory consulting

Principal Consultant - Health Economics & Modelling

ConsultingConfirmed live in the last 24 hours
Full-timeNo salary listedRemote

About the Job

Requirements

  • At least 10 years of health economics modelling experience, ideally including extensive consultancy experience.
  • Deep expertise across therapeutic areas, health technology assessment jurisdictions, and global market access.
  • Extensive experience as Project Director on complex, multi-jurisdictional projects.
  • Demonstrated experience supporting health technology assessment submissions, such as NICE, SMC, CADTH, and G-BA.
  • Proven track record of successful business development and account growth.
  • Demonstrated thought leadership through publications, presentations, or industry contributions.
  • Strong network within the pharmaceutical industry and the health technology assessment community.
  • Deep expertise in health economic modelling using Excel/VBA and R.
  • Advanced understanding of health technology assessment-relevant guidelines, techniques, and methodologies.
  • Proven ability to direct multiple projects in parallel.
  • Solid grasp of project financials, including pricing, work in progress, burn versus budget, and revenue recognition.
  • Advanced expertise in generative artificial intelligence tools for health economics modelling.
  • Exceptional client relationship and account management capabilities.
  • Proven influencing and negotiation skills, including discussing trade-offs and methodological decisions with senior client stakeholders.
  • Strategic business thinking and commercial acumen.
  • Strong written and oral communication across all organisational levels.
  • Results orientation and accountability.
  • Leadership, coaching, and team-building capabilities.
  • Ability to motivate teams, set clear expectations, and give constructive feedback.
  • Ability to remain calm under pressure and make pragmatic decisions in imperfect data environments.
  • Fluent English with a high degree of written accuracy.
  • A master's degree in health economics, economics, life sciences, mathematics, statistics, or a related quantitative discipline.

Responsibilities

  • Build and maintain relationships with clients.
  • Provide technical leadership and training to junior staff.
  • Generate and advocate thought leadership pieces.
  • Lead project delivery on time and to a high quality.
  • Write and present proposals to prospective clients.
  • Drive sales targets and new business activities.
  • Provide advanced methodological and modelling leadership on complex projects.
  • Act as Project Director on key engagements, ensuring quality, timelines, and financial performance.
  • Support account and client relationship management and contribute meaningfully to new business activities and business growth.
  • Take a visible role in developing people, methods, and internal standards.

Desired Qualifications

  • Extensive consultancy experience is ideal.
  • Experience coaching and line-managing, or de facto managing, junior staff is strongly preferred.
  • Additional European languages are advantageous.
  • Additional postgraduate training, such as a PhD or MBA, is advantageous but not essential.

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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