Oin our team of research analysts in clinical evidence analysis who research, analyze, and synthesize information and data about healthcare technologies and interventionsThis person will use the picots analytic framework to analyze published studies, assess strength of evidence (using the grade-based system), and write rapid and in-depth evidence assessments for ecris clinical evidence assessment membership servicesDecision makers, including clinical policy makers at third-party payers and health systems, use the assessments to make evidence-based decisions about appropriate use.
Reasonable accommodations statement
To accomplish this job successfully, an individual must be able to perform, with or without reasonable accommodation, each essential function satisfactorilyReasonable accommodations may be made to help enable qualified individuals with disabilities to perform the essential functions.
Essential functions statements(s)
Learn the appropriate methods for analyzing screening, diagnostic, and prognostic clinical studies Use search results provided by medical librarians to select appropriate data for analysis, perform analysis, and write evidence assessments Understand and apply concepts of picots analytic framework and grade strength of evidence assessment in report preparation Prepare for preliminary meetings on assigned topics and understand the patient clinical pathway for the screening, diagnosis, or management of the relevant disease/condition Ensure understanding of client research requests Meet deadlines for client deliverables Apply biostatistical concepts to accurately analyze and present data in the assessments Provide recommendations for prioritization of topics Understand factors that affect diffusion of drugs, devices, procedures, tests, and therapies Understand audience perspectives (e.g., payer, health system, patient) and write accordingly Write assessments clearly in active voice for intended audiences Use peer review feedback to revise assessments as needed after internal and external review; document responses to reviewers Use internal workflow tools (e.g., sharepoint) to follow appropriate procedures for report documentation, drafting, peer review, revision and final publication Attend training sessions for report writing and other ecri presentations that inform your work as recommended by management Maintain current knowledge of regulatory and reimbursement (coverage, coding, payment) issues and processes in the united states and abroad for drugs, devices, and procedures Maintain current awareness of important healthcare topics and issues by perusing major medical journals, health sections of newspapers, and the fierce family of daily healthcare publications on devices, pharma, and biotech Maintain general awareness of changes in codes (e.g., addition of new codes) used to bill and the policies affecting coverage/reimbursement of healthcare technology Maintain currency on state and federal regulatory issues affecting healthcare adoption of new technologies Be thorough and attentive to detail; document sources for all facts and information used in reports and use the internal citation system workflows to request and document resources used
Annual metrics after completing 9 months training:
Depending on the type and depth of assessments required by clients, produce some combination of the following as determined by client needs and management: 4 new or updated comprehensive in-depth assessments, or 40 rapid assessments, or 100 curated bibliographies, or combination of the three Identify recommended readings each week for client base Attend or contribute to relevant ecri webinars, conferences, trainings to grow/maintain knowledge base as recommended by management Professional development: if recommended and supported by budget and management, take relevant online education courses to grow your knowledge base
Strong writing skills coupled with familiarity with concepts of evidence-based medicine, systematic review, clinical study design and analysis of screening; biostatistics; issues related to diffusion of healthcare technology (regulatory and reimbursement issues in united states and abroad). Ability to: learn and use picots framework to formulate appropriate key questions; understand clinical trial design for diagnostic technologies and assess risk of bias in studies; clinical data analysis; apply grade concepts to assess strength of evidence and draw conclusions; if needed, perform basic statistical tests on study data, accept and appropriately implement peer review critiques; and write accurately and clearly for health plan and health system audiences. Preferred: basic knowledge about how third-party payer coverage decision-making works; familiarity with health technology assessment programs (e.g., agency for healthcare research and quality).
Education: phd+ post doc or 2 years research experience in a life science (e.g., human genetics, molecular biology, cell biology, virology, immunology) or ms degree in clinical research or life science, public health, or nursing +5 years experience
N (not applicable)
Activity is not applicable to this position.
Position requires this activity up to 33% of the time (0 - 2.5+ hrs/day)
Position requires this activity from 33% - 66% of the time (2.5 - 5.5+ hrs/day)
Position requires this activity more than 66% of the time (5.5+ hrs/day)