Research Specialist

Mass General Brigham•Boston, MA

3d•Hybrid

About The Position

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 in close-knit, internationally known research unit of 25+ Harvard faculty and 60+ support staff.

Requirements

Master's Degree Related Field of Study required
Experience in an academic or laboratory research setting 3-5 years required
Must be a problem solver willing to take the initiative and prioritize tasks, thereby ensuring the smooth and efficient conduct of several projects simultaneously.
A high degree of computer literacy in order to use various spreadsheet, database, accounting and word processing programs to assist in administrative, grant proposal preparation, and research reporting activities.
Excellent organizational skills in order to formulate, implement, and monitor a number of interrelated tasks.
Ability to exercise discretion and good judgment in handling of sensitive and confidential information.
Ability to work under deadline pressure and prioritize work from several sources.
Excellent interpersonal skills for internal and external communications.

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.
Conducts systematic reviews and helps oversee large prospective quality improvement trials being conducted to improve long-term medication adherence and health outcomes.
Contributes to the scientific literature through oral and poster presentations and published manuscripts.
Assists with grant proposals and project management, as needed.
Researches, develops, designs, and executes 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.