Consultant, Evidence Synthesis, Systematic Literature Review
Location: Mexico City, Mexico
Time Type: Full time
Job Description
Overview
Consultants are project delivery leaders who are responsible for implementing methodologically rigorous evidence synthesis research, managing the overall project, and overseeing the work of junior staff. They work independently and as part of a team, act on anticipated project needs, and proactively 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 design applicable projects.
Required Knowledge
Excellent knowledge of systematic literature review, narrative synthesis, and indirect treatment comparison. Fundamental understanding of SLR guidelines and best practices, and substantial experience in implementing them.
Responsibilities
Design and lead HTA compliant evidence synthesis studies, project management, and deliverable development
Must be able to efficiently implement SLRs and produce results with minimal errors
Understand how results can be used to support client’s business objectives
Synthesize data qualitatively
Manage staff to ensure high quality and timely work and review in detail the work that is produced
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
Essential Qualifications
PhD in epidemiology, pharmaceutical sciences, statistics (other health sciences ok)
Fluency in English (spoken and written)
3+ years’ experience of working in evidence synthesis research, preferably in consulting or academia
Essential General Technical Skills And Knowledge
Expert in evidence synthesis
Exceptional attention to detail a must
Strong scientific and logical writing with a track record of first author 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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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