BMC Software
Location
Boston, Massachusetts
Salary
$16 - $23 / HOUR
The Research Assistant will support clinical research activities by managing participant recruitment, scheduling visits, administering questionnaires, and extracting relevant data from medical records. This role also involves maintaining study databases and assisting with administrative and regulatory documentation for research operations.
A minimum of a Bachelor’s degree is required, preferably in science fields like chemistry or biology, along with prior clinical research or public health experience being preferred. Candidates must possess excellent communication skills and proficiency in Microsoft Office applications, while maintaining strict confidentiality.
The Research Assistant will support clinical research activities in the Waikar Research Group within the Nephrology Section. Responsibilities include participant recruitment and scheduling, administering questionnaires, reviewing medical records, managing study data, maintaining research databases, and assisting with administrative and regulatory tasks. The Research Assistant may also assist with basic bio specimen handling, sample processing in compliance with established protocols, and manuscript preparation. This role works closely with the Research Program Manager and other research staff to support research operations in both clinical and research settings.
The Research Assistant will support clinical research activities using approved techniques. Responsibilities include supporting participant recruitment and scheduling, administering questionnaires, reviewing participant charts and extracting relevant study data, maintaining participant databases, and assisting with preparation of reports and study documentation. This position requires comfort working in both clinical and research environments and collaborating as part of a team to support study participants and research operations. JOB RESPONSIBILITIES: Recruits and screens clinical research candidates. Interacts with participants by phone, email, and in person to support recruitment activities, study coordination, and visit scheduling. Completes informed consent documents and enrolls participants in the research protocol. The Research Assistant must be able to answer participant questions and explain the clinical trial in an easily understood and meaningful manner to participants. Collects, documents, and submits study data and samples accurately and efficiently. Works collaboratively with the Research Program Manager and other research staff to support daily study operation, ad hoc duties as assigned.
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