Senior Consultant, Evidence Synthesis, Indirect Treatment Comparison (ITC)

Senior Consultant, Evidence Synthesis, Indirect Treatment Comparison (ITC)Location: RemoteOVERVIEWSenior Consultants are project delivery leaders who are responsible for implementing methodologically rigorous evidence synthesis research, overseeing the work of junior staff, and managing the overall project. 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. Senior Consultants are expected to interact with clients, understand their needs and industry requirements, and design applicable projects.REQUIRED KNOWLEDGEExcellent 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.RESPONSIBILITIESDesign and lead HTA compliant evidence synthesis studies, project management, and deliverable developmentDevelop and execute analyses in RUnderstand how results can be used to support client’s business objectivesSynthesize data qualitativelyManage staff to ensure high quality and timely work and review in detail the work that is producedSupport more senior staff on specific business initiatives as requiredWork without supervision independently and/or as part of a project teamWork effectively across time zones as part of a global teamQUALIFICATIONS, EXPERIENCE, TECHNICAL AND PERSONAL SKILLSEssential qualificationsMasters in statistics, epidemiology, economics (other health sciences ok)5+ years’ experience of working in evidence synthesis research, preferably in consulting or academiaPreferred experiencePhD in statistics, epidemiology, economics (other health sciences ok)Essential general technical skills and knowledgeProficient programming skills in RExpert in evidence synthesisExceptional attention to detailStrong scientific and logical writing with a track record of first author conference abstracts and manuscriptsStrong ability to quality check own and others work so that drafts are delivered with only minimal minor typographical errorsEssential personal skills and behaviorsFluency in English (spoken and written)A commitment to working collaboratively and effectively with others in and across the team to accomplish goalsA commitment to timely internal and client communicationA pragmatic and logical problem solving approach to projectsStrong attention to detail on all project deliverables even under time pressureA good understanding of project management with proven time management and personal organizational skillsIQVIA 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.We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.The potential base pay range for this role, when annualized, is $151,200.00 - $252,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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