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Global drug and device development services

Lead Consultant: Systematic Reviews/Evidence Synthesis

ConsultingConfirmed live in the last 24 hours
Full-timeReading, UK

About the Job

Requirements

  • A Master's degree or higher (PhD) in public health, health economics or a related quantitative discipline, such as operational research, medical statistics, or epidemiology, or a clinical degree such as MD or PharmD.
  • Experience designing and leading systematic literature reviews, targeted literature reviews, and/or evidence synthesis.
  • Significant relevant industry or consultancy experience; consultancy experience is preferred.
  • Demonstrable people-management experience.
  • Demonstrable business-development experience.
  • Significant experience in a consulting, academic, pharmaceutical, or medical-device industry environment.
  • Proven management experience, particularly the ability to lead a team of junior analysts.
  • Ability to work effectively as part of a team.
  • High self-motivation.
  • Leadership potential.
  • Legal right to work in the country where the role is based.

Responsibilities

  • Act as project director and manage all aspects of systematic literature reviews and/or evidence synthesis, including network meta-analyses and indirect treatment comparisons, ensuring deliverables meet client requirements.
  • Establish and maintain client relationships and lead proposal development for systematic literature reviews and targeted literature reviews.
  • Oversee resourcing, staff development, recruitment activities, and departmental growth within the practice.
  • Contribute strategically and lead business development and proposal processes.
  • Provide technical mentorship to junior reviewers, identify and manage training needs, and provide on-the-job training and support as required.
  • Lead publications and scientific communications for self and department staff.
  • Direct, manage, and participate in proposal writing, project work, and client liaison.
  • Support senior leadership in implementing business strategies for the practice.
  • Form part of the global practice management team and participate in day-to-day management of the group.
  • Promote an open and honest working environment.
  • Travel approximately 15% domestically or internationally.

Desired Qualifications

  • Consultancy experience.

About the Company

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Global drug and device development services

This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.

Company size
10,001+
Company stage
IPO
Headquarters
Ireland
Founded
1990

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