T229 - Rwe Analyst - Observational Studies & Evidence

As an Analyst within the Real World Evidence Department, you will have a key role within the HEOR practice. You are expected to be capable of working on different projects and types of work (across the COEs), so a flexible, enthusiastic, and professional approach is essential. A good knowledge of HEOR methods/approaches plus a working knowledge of consulting methodologies and general business practices is required, as well as an understanding of the healthcare sector and the pharmaceutical market, gained through the delivery of consulting engagements (if possible).General ResponsibilitiesCarry out work to a high standard which meets or exceeds client expectationsSupport senior staff on specific business initiatives as requiredWork independently and/or as part of a project team on defined tasks:Project managementAssist with overall project/client managementAttend client and other external meetings as appropriateManage specific project work streams independentlyLiterature and data reviewDevelop search strategies for structured and systematic literature reviewsManage the full review process (abstract review, paper selection, and data extraction)Write and review literature review reportsOutcomes Research - Observational StudiesHelp in designing data collection forms, known as case report forms (CRFs)Coordinate with the ethics committeeIdentify/select an investigator who will be responsible for the conduct of the study at the study siteEnsure that investigators and the sites where the research is to be performed are adequate to the purposes of the studyLiaise with doctors/consultants or investigators on conducting the studyObtain investigators' compromise before sending the study materialsMonitor the study throughout its duration, which involves visiting or contacting the study sites on a regular basis, or performing remote monitoring activitiesEnsure that storage, distribution, return procedures, and documentation for the study are secure and adequateVerify that data entered onto the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV)Collect completed CRFs from hospitals and general practicesPerform follow-up on Data Management or SAE (safety) queriesSend regular study reports to the sponsor, in accordance with the agreed scheduleWrite visit reports and file and collate study documentation and reportsClose down study sites on completion of the studyArchive study documentation and correspondenceCoordinate investigator paymentOccasionally write manuscripts for publicationQualificationsMHA/MPH/PhD - education in health science, public health, health services research, or a relevant related areaClinical trials monitoring knowledgePrevious work experience in outcomes research/RWE/evidence generationStrong qualitative and quantitative skillsFamiliarity with Microsoft Office package#J-18808-Ljbffr