Senior Consultant, Evidence Synthesis in RWE

1 month ago

Mississauga, Ontario, Canada IQVIA Full time

Lead Consultant, Evidence Synthesis, RWE

OVERVIEW

The Lead Consultant plays a pivotal role in managing projects that involve methodologically sound evidence synthesis research. This position requires overseeing junior team members and ensuring the successful execution of the overall project. The individual must demonstrate strong organizational skills, meticulous attention to detail, and effective communication abilities. Engaging with clients to understand their needs and designing pertinent projects is a critical aspect of this role.

ESSENTIAL SKILLS

A comprehensive understanding of systematic literature review (SLR) methodologies and indirect treatment comparisons, including network meta-analysis (NMA) and matching-adjusted indirect comparison (MAIC), is essential. Familiarity with SLR guidelines and best practices, along with significant experience in their application, is required. Proficiency in conducting indirect treatment comparisons using R, STATA, or SAS is mandatory.

KEY RESPONSIBILITIES

  • Develop evidence synthesis studies that adhere to health technology assessment (HTA) standards, manage project timelines, and produce deliverables
  • Demonstrate an exceptional ability to interpret observational and clinical trial study designs, as well as analyze statistical results in published literature
  • Conduct qualitative and quantitative data synthesis
  • Supervise team members to ensure high-quality output and meticulously review their work
  • Provide support to senior staff on specific business initiatives as required
  • Operate independently or collaboratively within a project team on designated tasks
  • Effectively collaborate across different time zones as part of a global team

QUALIFICATIONS AND EXPERIENCE

  • Master's degree (required) or PhD (preferred) in epidemiology, pharmacology, public health, or biostatistics (other health sciences acceptable)
  • Over 5 years of experience in evidence synthesis research, ideally within consulting, pharmaceutical, or healthcare sectors, and substantial experience in independently conducting meta-analyses and indirect treatment comparisons in at least one programming language; a minimum of 2 years in a client-facing role managing project delivery
  • Expert-level knowledge of evidence synthesis methodologies
  • Exceptional attention to detail and quality assurance skills
  • Strong scientific writing capabilities, with a proven track record as a primary author of conference abstracts and manuscripts
  • Ability to conduct thorough quality checks on personal and team outputs to ensure minimal errors
  • Proficiency in English, both spoken and written
  • Commitment to effective teamwork and achieving collective goals
  • Dedication to timely communication with internal teams and clients
  • Logical and strategic problem-solving skills in project contexts
  • Strong organizational skills with a focus on detail in all project deliverables, even under tight deadlines

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to advancing human science and data science to create a healthier world. Learn more at

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