Analyst, Real World Evidence

at  IQVIA

Job Overview
Analysts are key team members who are responsible for implementing methodologically rigorous evidence synthesis research under the guidance of senior staff. They work independently and as part of a team, act on anticipated project needs, and problem solve.

Responsibilities

• Synthesize data quantitatively (meta-analysis and NMA) and qualitatively with minimal supervision.
• Take responsibility for SLR related tasks including developing search strategies, protocols, analytic plans, and quality control. Deliver quality that exceeds client’s expectations.
• Assisting in preparation of abstracts, manuscripts and oral presentations, including development of slides and posters for presentation of project results at conferences.
• Drafting significant sections of study protocols, reports, and other client facing documents.
• Organizing and help manage research projects.
• Reviewing and providing relevant epidemiological and project-specific comments to statistical analysis plans and analysis output.
• Reviewing and providing input for scientific tasks including CRF/eCRF development, form previews and other ad hoc project tasks (e.g., regulatory responses, slide deck development).
• Actively participating in client-facing project meetings and being a recognized member of the project team.
• Conduct statistical analysis as needed.
• Write reports and develop slide decks on methods and results.
• Help prepare proposal drafts, including background research and writing methods sections.
• Work without supervision independently and/or as part of a project team on defined tasks.
• Assist with overall project management and client management.

Required knowledge
Excellent knowledge of systematic literature review (SLR) methods, guidelines and best practices. Experience conducting meta-analysis, network meta-analysis (NMA), and/or experience with Bayesian analysis, using R, STATA, or SAS. Must have advanced statistical training or equivalent experience, and comfortable with conducting analyses independently.

Qualifications

• Master´s degree in epidemiology, biostatistics, pharmacology, or public health
• 3+ years’ of working experience in evidence synthesis research, preferably in consulting, pharmaceutical or other healthcare industry, academia.
• Strong quantitative background with a demonstrated ability to independently conduct analyses using a statistical program (e.g., meta-regression, multivariate regression)
• Exceptional attention to detail
• Strong ability to interpret results and strategically apply them to support client’s needs
• Solid understanding of SLR concepts, guidelines, and required rigor
• Competency in using PowerPoint, Excel, Word, and one statistical program
• Fluency in English (spoken and written); strong business/scientific written English
• A pragmatic and logical problem solving approach to projects
• A good understanding of project management with proven time management and personal organizational skills
• A commitment to working collaboratively and effectively with others in and across the team to accomplish goals.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.co

• Synthesize data quantitatively (meta-analysis and NMA) and qualitatively with minimal supervision.
• Take responsibility for SLR related tasks including developing search strategies, protocols, analytic plans, and quality control. Deliver quality that exceeds client’s expectations.
• Assisting in preparation of abstracts, manuscripts and oral presentations, including development of slides and posters for presentation of project results at conferences.
• Drafting significant sections of study protocols, reports, and other client facing documents.
• Organizing and help manage research projects.
• Reviewing and providing relevant epidemiological and project-specific comments to statistical analysis plans and analysis output.
• Reviewing and providing input for scientific tasks including CRF/eCRF development, form previews and other ad hoc project tasks (e.g., regulatory responses, slide deck development).
• Actively participating in client-facing project meetings and being a recognized member of the project team.
• Conduct statistical analysis as needed.
• Write reports and develop slide decks on methods and results.
• Help prepare proposal drafts, including background research and writing methods sections.
• Work without supervision independently and/or as part of a project team on defined tasks.
• Assist with overall project management and client management