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. Understanding of the health care sector and the pharmaceutical market, gained through the delivery of consulting engagements (if possible).General Responsibilities Carry out work to a high standard which meets or exceeds client expectations.Support senior staff on specific business initiatives as required.Work 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 review:Develop 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 Studies:Helping in designing data collection forms, known as case report forms (CRFs)Coordinating with the ethics committeeIdentifying/selecting an investigator who will be responsible for the conduct of the study at the study siteEnsuring that investigators and the sites where the research is to be performed are adequate to the purposes of the studyLiaising with doctors/consultants or investigators on conducting the studyObtaining investigators' compromise before sending the study materialsMonitoring the study throughout its duration, which involves visiting or contacting the study sites regularly, or performing remote monitoring activitiesEnsuring that storage, distribution, return procedures, and documentation for the study are secure and adequateVerifying that data entered onto the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV)Collecting completed CRFs from hospitals and general practicesPerforming follow-up on Data Management or SAE (safety) queriesSending regular study reports to the sponsor, in accordance with the agreed scheduleWriting visit reports and filing and collating study documentation and reportsClosing down study sites on completion of the studyArchiving study documentation and correspondenceCoordinating investigator paymentOccasionally writing manuscripts for publicationQualifications MHA/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
