Research Specialist/ day/ 40 hrs/ DOM Pharmacoepidemiology (PORTAL)
Brigham & Women's Hospital(BWH)

Job Info

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General Overview:

Functioning under the direction of the principal investigators and other faculty members, the Research Specialist works independently to conduct high level, complex research study design and analysis in the areas of pharmacoepidemiology, epidemiology/biostatistics, and analytic methods. Contributes to scientific literature, reports, journals, manuscripts (including co-authorship as appropriate), presentations, and grant writing. Work remotely and/or in buisiness casual offie environment in close-knit, internationally known research unit of 20 Harvard faculty and 40 support staff. This particular RS will focus mainly on the PORTAL group within the division which has distinct characteristics of their own.

Principal Duties and Responsibilities:

Under the direction of principal investigators, assists in the designing, planning, and execution of analyses of therapeutic outcomes and adverse effects of drugs and other medical interventions, as well as simulation studies evaluating epidemiologic methods and validation studies in claims data; applying skills in biostatistics, epidemiologic methods, and health services research. Serves as an integral part of the research team, helps to analyze and interpret data findings, prepare summaries, reports and presentations based on analysis and results. The Research Specialist will also help oversee large prospective quality improvement trials being conducted to improve long-term medication adherence and health outcomes. The Research Specialist will work with the principal investigators to review available clinical evidence. Contributes to the scientific literature through oral and poster presentations and published manuscripts. Assists with grant proposals and project management, as needed.

Specific Duties Include, but are not limited to:

Researches, develops, designs and executes and interprets research data

Contributes to interpretation of research data and results

Contributes to scientific literature, journals, and oral presentations

Participate in study design and protocol development

Participate in Institutional Review Board (IRB) submission process for new research protocols

Take part in design and writing of grant proposals and grant material

Compose and present sections of research reports and manuscripts

Perform advanced data analysis, working closely with the Principal Investigator and other researchers

Performs other duties as assigned

Works within legal, regulatory, accreditation and ethical practice standards relevant to the position and as established by BWH/Partners; follows safe practices required for the position; complies with appropriate BWH and Partners policies and procedures; fulfills any training required by BWH and/or Partners, as appropriate; brings potential matters of non-compliance to the attention of the supervisor or other appropriate hospital staff

Qualifications
Qualifications:

• MS/MD/PHD/PharmD or equivalent degree in Epidemiology, Biostatistics, or related field; emphasis on methods and or pharmaco-epidemiology preferred; healthcare-related doctoral degree a plus

• Ideally 10 plus years of relevant experience
• Excellent knowledge of epidemiologic methods; focus on Pharmacoepidemiology desirable
• Experience in research using large claims databases
• Experience in collaborative projects with clinical medicine is preferred
• Knowledge and skills in the critical appraisal of research evidence are highly desired
• Background in pharmaceuticals is advantageous

Skills:

The successful candidate will have very good methodologic and analytic skills in epidemiology to help implement these research projects, with knowledge of pharmacoepidemiology an added advantage. The study of large longitudinal claims data and the analysis of correlated discrete data structures requires experience and substantial skills in this research. The candidate must have the abilities to independently design and analyze complex epidemiologic claims data analyses, to perform major database manipulation and statistical analyses in SAS or other statistical package, and to draft study reports for funding agencies. Strong time management/organizational skills as well as written and verbal presentational skills are necessary. An understanding of clinical medicine is an advantage but not required. Familiarity with pharmaceuticals is desirable.

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