Senior Clinical Research Coordinator, PD
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![]() United States, Massachusetts, Boston | |
![]() 1620 Tremont Street (Show on map) | |
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Principal duties may vary depending on the phases of the project (e.g., intervention development, data analysis, dissemination activities). The (candidate) will assist and facilitate all activities associated with the execution of the research plan, including study design, development of quality improvement/patient safety interventions, oversight of data collection and data management, generation of regular progress reports, organizing communication with participants and project staff (e.g., meeting agendas and minutes, tasks to be completed), and oversight/supervision of research assistants. Depending on the study, the (candidate) may recruit patients for trials, verify inclusion/criteria, obtain informed consent, administer surveys to study subjects by phone or in person, and/or abstract data from electronic health records. The (candidate) will use a variety of tools to help collect and manage data (e.g., Microsoft Excel, MS Access, REDCap) and tools to facilitate project management and timelines (e.g., MS Teams, Trello). The (candidate) will facilitate data analysis and participate in dissemination activities, including feedback reports to study participants, funders, and oversight agencies, and assist with developing scientific abstracts, manuscripts, and presentations at local and national meetings and conferences. The (candidate)'s responsibilities may also include a limited amount of time on administrative tasks, literature searches, synthesizing research, as well as supporting the research team with project management, including the development and documentation of protocols, assisting with formal audits of data and other regulatory requirements, training other staff, and communicating requirements to study teams.
The (candidate) will be required to work closely with investigators and staff at BWH, Mass General Brigham as well as outside institutions. This position requires excellent interpersonal skills, writing skills, problem-solving skills, and strong organizational and communication skills. An understanding of health information technology and digital health development is preferred. Principal duties may vary depending on the phases of the project (e.g., intervention development, data analysis, dissemination activities). The (candidate) will assist and facilitate all activities associated with the execution of the research plan, including study design, development of quality improvement/patient safety interventions, oversight of data collection and data management, generation of regular progress reports, organizing communication with participants and project staff (e.g., meeting agendas and minutes, tasks to be completed), and oversight/supervision of research assistants. Depending on the study, the (candidate) may recruit patients for trials, verify inclusion/criteria, obtain informed consent, administer surveys to study subjects by phone or in person, and/or abstract data from electronic health records. The (candidate) will use a variety of tools to help collect and manage data (e.g., Microsoft Excel, MS Access, REDCap) and tools to facilitate project management and timelines (e.g., MS Teams, Trello). The (candidate) will facilitate data analysis and participate in dissemination activities, including feedback reports to study participants, funders, and oversight agencies, and assist with developing scientific abstracts, manuscripts, and presentations at local and national meetings and conferences. The (candidate)'s responsibilities may also include a limited amount of time on administrative tasks, literature searches, synthesizing research, as well as supporting the research team with project management, including the development and documentation of protocols, assisting with formal audits of data and other regulatory requirements, training other staff, and communicating requirements to study teams. PRINCIPAL DUTIES AND RESPONSIBILITIES: Indicate key areas of responsibility, major job duties, special projects and key objectives for this position. These items should be evaluated throughout the year and included in the written annual evaluation. The exact responsibilities will vary by project and may include the following:
For all positions that include direct patient care, indicate with an "X" the age(s) of all patient populations served No Direct Patient Care X All age groups Adolescence (13 to 17 years) Neonates (birth to 1 month) Young Adult (18 to 25 years) Infant (1 month to1year) Adult (26 to 54 years) Early Childhood (12 months to 5 years) Senior Adult (55 to 64 years) Late Childhood (6 to 12 years) Geriatric (65 years and up) QUALIFICATIONS: (MUST be realistic, neither overstated nor understated, and related to the essential functions of the job.)
JOB SPECIFIC SKILLS/ ABILITIES/ COMPETENCIES REQUIRED: (MUST be realistic, neither overstated nor understated, and related to the essential functions of the job.)
WORKING CONDITIONS: Describe the conditions in which the work is performed. Professional office and clinical setting. The Brigham and Women's Hospital, Inc. is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. |