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
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