Principal Consultant
Parexel
Principal Consultant
Parexel
End-to-end clinical trials and regulatory consulting
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Job Purpose:
As a senior leader a Principal Consultant in the HEOR modelling team has responsibility for building and maintaining relationships with clients, for providing technical leadership and training to junior staff, generating and advocating thought leadership pieces, and for leading the delivery of projects on time and to a high quality. In addition, the Principal Consultant has an important role in writing and presenting proposals to prospective clients, driving sales targets and NBA's.
Principal Consultants are senior technical and project leaders in the Health Economics & Modelling (HEM) team, with key responsibilities including;
· Providing advanced methodological and modelling leadership on complex projects
· Acting as Project Director on key engagements, assuring quality, timelines and financial performance
· Support account and client relationship management and contribute meaningfully to new business activities, driving business growth
· Take a visible role in developing people, methods, and internal standards
Essential Knowledge & Experience You Will Require For This Role:
· 10-15+ years of health economics modelling experience, ideally with extensive consultancy experience
· Deep expertise across therapeutic areas, HTA jurisdictions and global market access
· Extensive experience as Project Director on complex, multi-jurisdictional projects
· Demonstrated experience supporting HTA submissions (e.g. NICE, SMC, CADTH, G-BA, others)
· 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 HTA community
· Experience coaching and line-managing (or de facto managing) junior staff is strongly preferred.
Skills Required:
· Deep expertise in health economic modelling (Excel/VBA, R)
· Advanced understanding of HTA-relevant guidelines, techniques and methodologies
· Proven ability to direct multiple projects in parallel
· Solid grasp of project financials (pricing, WIP, burn vs. budget, revenue recognition)
· Advanced expertise in generative AI tools for health economics modelling
· Exceptional client relationship and account management capabilities
· Proven influencing and negotiation skills, comfortable in discussing trade-offs and methodological decisions with senior client stakeholders
· Strategic business thinking and commercial acumen
· Outstanding written and oral communication across all organisational levels
· Results-oriented with a strong accountability mindset
· Leadership, coaching, and team-building capabilities
· Ability to motivate teams, set clear expectations, and give constructive feedback
· Calm under pressure; able to make pragmatic decisions in imperfect data environments
· Fluent English with a high degree of written accuracy; additional European languages advantageous
Education Requirements for this role:
· Master's degree in health economics, economics, life sciences, mathematics, statistics, or related quantitative discipline.
· Additional postgraduate training (e.g. PhD, MBA) is an advantage, but not essential.
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.
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