Established in 2005 as a joint initiative of Harvard Medical School (HMS) and the Harvard School of Public Health (HSPH), CSPH's (Center for Surgery and Public Health) mission is to advance the science of surgical care delivery by studying effectiveness, equity, and value at the health system and population levels, to inform policy, and to provide support for faculty and trainees committed to excellence in surgical health services research (HSR). CSPH's expertise in HSR also informs its work in addressing the burden of surgical disease in lower and middle-income countries and resource-limited settings.
The RA II will primarily be involved in a study we are conducting that uses case studies at different healthcare systems across the US as a part of a NIH-funded study focused on advanced care planning (ACP) discussions between patients and their doctors. ACP refers to discussions around patient values and preferences for their care as they become seriously ill, including end of life discussions. This study uses both quantitative and qualitative methods, including quantitative data analysis of Medicare claims data and qualitative data collection through interviews, case studies and focus groups. The RA will be involved with other studies or projects as they arise.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
Provides assistance on clinical research studies as per study guidelines and protocols.
Recruits and evaluates potential study participants. Per study protocol, conducts interviews or schedules patients for study visit and screening.
Communicates study information to patient participants via phone and mail, including patient education, informational packets, procedural instruction, follow-up. May serve as a liaison between patient and physician.
Collects data and maintains confidential patient records and participant database. May be required to input data, conduct basic analyses and run various reports.
Answers any phone calls and inquiries regarding study protocol. Refers participants when appropriate to supervisor or clinical staff.
Monitors and sets up any needed equipment in the office.
Maintains regulatory documents and IRB as needed.
All other duties, as assigned.
Bachelor's degree required, Master's preferred.
At least one year experience and have demonstrated sounds independent judgement and competencies in research methodologies.
Excellent interpersonal skills are required for working with the study participants.
Good oral and written communication skills.
Careful attention to detail.
Excellent organizational skills and ability to prioritize a variety of tasks.
Ability to demonstrate professionalism and respect for subjects' rights and individual needs.
Familiarity with Microsoft Office suite (Word, Excel, Outlook).
Knowledge of clinical research protocols.
Knowledge of data collection and analysis programs (such as REDCap, Stata, Atlas.ti, SAS).
Previous experience consenting study participants.
Previous interaction with patients and families.
Will be based in a Partners facility and will directly interact with the project team members. Will also have opportunities to engage in work-related travel, and to attend research meetings, webinars and sessions, as appropriate.
Partners Healthcare System