**OVERVIEW** Consultants are doers and have a strong appetite for learning. They are key members of the Evidence Synthesis practice and, under the supervision of more senor staff, are responsible for implementing methodologically rigorous evidence synthesis research and developing high quality deliverables on time. They work independently and as part of a team, act on anticipated project needs, and problem solve. The role requires superb attention to detail, organization skills, and communication skills. Consultants are expected to interact with clients, understand their needs and industry requirements, and develop applicable deliverables. **REQUIRED KNOWLEDGE** Excellent knowledge of statistical methods for indirect treatment comparison, including network meta-analysis (NMA), multilevel network meta-regression, simulated treatment comparison, and matching-adjusted indirect comparison (MAIC). Fundamental understanding of SLR guidelines and best practices, and substantial experience in implementing them. Hands on experience conducting Bayesian analyses and ITCs in R is a must. **RESPONSIBILITIES** Implement HTA compliant evidence synthesis studies, project management, and deliverable development + Develop and execute analyses in R + Understand how results can be used to support client’s business objectives + Synthesize data qualitatively + Develop SLR protocols, screen, extract data, and write reports + Support more senior staff on specific business initiatives as required + Work without supervision independently and/or as part of a project team + Work effectively across time zones as part of a global team **QUALIFICATIONS, EXPERIENCE, TECHNICAL AND PERSONAL SKILLS** + PhD in epidemiology, pharmacology, public health, or biostatistics (other health sciences ok) + 3+ years of experience of working in evidence synthesis research at a consulting firm, preferred + 2+ years independently conducting ITC in R + 2+ years of experience developing deliverables of those projects + Advanced English (must be able to be comfortable in client facing meetings as well as technical language) + Proficient programming skills in R + Expert in evidence synthesis + Exceptional attention to detail + Strong scientific and logical writing with a track record of first author conference abstracts and manuscripts + Strong ability to quality check own and others work so that drafts are delivered with only minimal minor typographical errors IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled