As an Associate Consultant, you will be involved in the production of systematic literature reviews (SLRs), through the analysis of large volumes of qualitative and quantitative health care data, combined with the interpreting and critically evaluating the retrieved evidence.
You will also support various project-related activities as per requirements and perform literature review using interfaces such as PubMed, Embase, and Cochrane, whilst ensuring on-time delivery of SLR/TLR support assignments. Additionally, you will be required to contribute to CoE and other team initiatives.
Requirements:
2 - 4 years of prior relevant experience or equivalent
Bachelor's Degree or equivalent in life sciences related discipline or related field (MBBS, B
Pharm, BDS)
Good knowledge of database and literature searches
Good understanding of common statistical methods used in clinical trials and/or interpretation of their results
Good understanding of statistical principles and of medical terminology across a range of therapeutic areas
Good knowledge of title and abstract screening, article download, and full-text screening activities
Good knowledge of performing critical appraisal activities as involved in conducting a SLR
Skilled with Microsoft Word and proficient Microsoft Excel
Excellent presentation skills, including knowledge of PowerPoint
Excellent verbal and written communication
High levels of organisation and attention to detail
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
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