Executive Director, Evidence Synthesis & Statistics in Manchester

RTI Health Solutions (RTI-HS), a wholly owned subsidiary of RTI International, is an independent and internationally recognized research organization. With offices in the US, UK, Spain, France, and Sweden, we provide healthcare consulting and research expertise to optimize decision making for pharmaceutical, biotechnology, and medical device products across the development and marketing lifecycle. Clients rely on our expertise, quality standards, and integrity to guide their product development and regulatory and market access strategies. Our various practice areas include Value, Access, and HEOR; Patient-Centered and Outcomes Research; Epidemiology and Biostatistics; Medical Communications; Global Business Operations; and Strategic Consulting and Growth.

The Evidence Synthesis & Statistics (ESS) capability plays an important role in helping clients evaluate the clinical, humanistic, and economic value of healthcare interventions. The team delivers evidence synthesis, advanced statistical analysis, and strategic evidence planning to support HTA, regulatory, payer, market access, and evolving Joint Clinical Assessment (JCA) decision-making globally.

We are seeking an accomplished scientific leader to lead and grow RTI-HS’s ESS capability. This individual will provide strategic, scientific, and operational leadership for evidence synthesis and statistical services while remaining hands-on in the delivery of complex client work.

Location: We offer flexible working arrangements for this position, which can be based in our Manchester office, fully remote within the UK, or from one of our other European office locations in Spain, Sweden, or France.

What You'll Do

• Provide scientific, strategic, and operational leadership for RTI-HS’s evidence synthesis services.
• Lead and grow RTI-HS’s Evidence Synthesis & Statistics capability, establishing a market-leading practice focused on evidence generation, advanced analytics, and decision support.
• Serve as a senior scientific advisor to pharmaceutical and biotechnology clients on evidence synthesis methodologies and evidence generation strategy.
• Provide technical leadership, hands-on methodological input, and quality assurance across a wide range of evidence synthesis activities.
• Lead and directly contribute to complex analytical work, including projects involving Bayesian methods, causal inference, patient-reported outcomes analysis, survival analysis, mixed effects/hierarchical modeling, network meta-analysis, and other indirect treatment comparisons.
• Advise on integrated evidence strategies aligning clinical development, HEOR, RWE, market access, and publication objectives.
• Drive innovation in methods, ensuring adoption of new and evolving approaches and continuous improvement in delivery.
• Lead business development activities, including identifying opportunities, developing proposals, supporting client presentations and scientific meetings, and contributing senior scientific insight throughout the sales process.
• Partner with commercial and scientific leaders across RTI-HS to expand the visibility and position of the ESS capability.
• Act as a senior client contact, building long-term relationships and providing strategic and methodological input across engagements.
• Monitor industry trends, HTA, payer, and evolving JCA evidence requirements, and competitive landscape to inform service development.
• Build, mentor, coach, and develop a high-performing team of evidence synthesis statisticians.
• Oversee project delivery to ensure scientific rigour, client satisfaction and financial performance.
• Lead complex projects and portfolios, ensuring alignment to timelines, budgets, quality standards, and client expectations.
• Ensure appropriate tools, processes, and methodological standards are in place and continuously improved.
• Foster collaboration across HEOR, RWE, Epidemiology, Market Access and Biostatistics to deliver integrated solutions.
• Represent RTI-HS through conference presentations, publications, workshops and webinars.
• Build the external scientific profile of the ESS capability through active engagement with the research and HTA community.
• Contribute to the advancement of evidence synthesis methodologies, promoting innovative approaches that leverage AI, automation, advanced analytics, and other emerging technologies where appropriate.
• Support development of internal best practices, methodological guidance and reusable intellectual capital.

What You'll Need

• Advanced degree (Masters, PhD, DrPH, ScD, MD, PharmD, or equivalent) in epidemiology, health economics, biostatistics, public health, pharmacy, or a related scientific discipline, plus a minimum of 12+ years of relevant experience.
• Significant relevant experience leading evidence synthesis activities within a pharmaceutical company, CRO, consulting organisation, or academic research environment.
• Demonstrated success leading multidisciplinary project teams and managing complex client engagements.
• Proven business development experience, including proposal leadership, client relationship management and revenue generation.
• Strong expertise across advanced statistical and evidence synthesis methodologies, including Bayesian approaches, network meta-analysis, other indirect treatment comparisons, survival analysis and health utility analysis.
• Familiarity with emerging methods and approaches, such as target trial emulation and evolving evidence synthesis techniques.
• Advanced programming skills in R and/or STATA.
• Strong understanding of global HTA, payer, and evolving JCA evidence requirements, and the role of evidence synthesis across the product lifecycle.
• Exceptional communication and presentation skills, with the ability to engage scientific, commercial and executive audiences.