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 management Assist with overall project/client management Attend client and other external meetings as appropriate Manage specific project work streams independently Literature and data review: Develop search strategies for structured and systematic literature reviews Manage the full review process (abstract review, paper selection, and data extraction) Write and review literature review reports Outcomes Research - Observational Studies: Helping in designing data collection forms, known as case report forms (CRFs) Coordinating with the ethics committee Identifying/selecting an investigator who will be responsible for the conduct of the study at the study site Ensuring that investigators and the sites where the research is to be performed are adequate to the purposes of the study Liaising with doctors/consultants or investigators on conducting the study Obtaining investigators' compromise before sending the study materials Monitoring the study throughout its duration, which involves visiting or contacting the study sites regularly, or performing remote monitoring activities Ensuring that storage, distribution, return procedures, and documentation for the study are secure and adequate Verifying 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 practices Performing follow-up on Data Management or SAE (safety) queries Sending regular study reports to the sponsor, in accordance with the agreed schedule Writing visit reports and filing and collating study documentation and reports Closing down study sites on completion of the study Archiving study documentation and correspondence Coordinating investigator payment Occasionally writing manuscripts for publication Qualifications MHA/MPH/PhD - education in health science, public health, health services research, or a relevant related area Clinical trials monitoring knowledge Previous work experience in outcomes research/RWE/evidence generation Strong qualitative and quantitative skills Familiarity with Microsoft Office package #J-18808-Ljbffr
