2 days ago
• Conduct Systematic Reviews (mostly rapid reviews) of high-priority pharmacologic and device-safety topics • Ability to work independently to take a project conception through protocol development phase, execution of the protocol, and final report submission within the project deadline • Conduct rapid systematic reviews of varying scope • Ensure understanding of client needs and scope for a variety of client requests • Develop key questions and implement the research protocol including PICOTS • Collaborate with information-retrieval specialists on conducting appropriate search strategies • Use search results to identify and select appropriate clinical literature to address key questions • Screen title/abstracts – sometimes several thousand references – for inclusion based on the PICOTs framework • Abstract study data into data tables • Mastery at assessing risk-of-bias, familiarity with relevant tools • Mastery in recognizing a variety of study designs • Ability to interpret statistical results accurately • Experience with GRADE system for assessing the strength of a body of evidence • Excellent writing skills/ability to summarize the reports results in narrative form • Ability to work well alone or in small groups, as dictated by the project’s needs • Ability to handle multiple projects simultaneously
• Masters Degree, or higher in social sciences, epidemiology, biology/chemistry, or other related fields • Minimum 5 years' experience conducting Systematic Reviews • Prior experience performing Systematic Reviews as project/methodological lead • Must have led at least 5 complete systematic reviews from inception to completion • Demonstrated qualitative and analytical skills with a strong understanding of statistical and research methodology • Strong analytical, critical thinking and communication skills including technical writing and editing • Demonstrated ability to guide team members through systematic review methodology • Knowledge or expertise with pharmaceutical and health care device safety topics preferred • Previous experience working and/or collaborating with researchers from federal government agencies whose mission relates to public health (e.g., NIH, CDC, FDA, HRSA, or other HHS agencies)
• Health Insurance • Dental Insurance • Vision insurance • Health Spending Account • Flexible Spending Account • Life and Disability insurance • 401(k) plan with company match • Paid Time Off (Vacation, Sick Leave and Holidays) • Education and Professional Development Assistance • Remote work from anywhere within the continental United States
Apply Now6 days ago
Facilitates coding research and guidelines development for Advocate Health's revenue cycle operations. Leverages coding expertise to ensure compliance with updated regulations.
🇺🇸 United States – Remote
💵 $29 - $44 / hour
💰 $10.2M Grant on 2019-08
⏰ Full Time
🟡 Mid-level
🟠 Senior
🔬 Research Analyst
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