Research Assistant I, Center for Surgery & Public Health

Mass General BrighamBoston, MA
Hybrid

About The Position

The Research Assistant I will play a key role in two high-impact research studies. The first study investigates access to and the quality of services provided by the State Health Insurance Assistance Program (SHIP), which delivers free, critical education and counseling on Medicare coverage options to beneficiaries and their families. This mixed-methods study integrates rigorous quantitative analysis of prospectively collected data with in-depth qualitative research using semi-structured interviews to explore user experiences and system performance (75%). The second study is a qualitative investigation into the goals and decision-making priorities surrounding surgery for advanced cancer, incorporating perspectives from patients, caregivers, surgeons, and oncologists. This project involves direct clinic-based observations and comprehensive interviews to capture the nuances of care at the intersection of oncology and palliative surgery. (25%) The RA II may also contribute to additional studies or initiatives as they develop, supporting the broader research mission of the team.

Requirements

  • Bachelor’s degree required.
  • 0-1 yrs of experience.
  • Excellent interpersonal skills are required for working with the study participants.
  • Good oral and written communication skills.
  • Knowledge of computer programs such as excel, word, outlook etc.
  • Excellent organizational skills and ability to prioritize a variety of tasks.
  • Careful attention to detail.
  • Ability to demonstrate professionalism and respect for subjects’ rights and individual needs.

Nice To Haves

  • 2 years of experience or master’s degree preferred.

Responsibilities

  • Conducts research studies as per study guidelines and protocols.
  • Recruits and evaluates potential study participants.
  • Per study protocol, conducts interviews following a semi-structured guide or schedules interviews.
  • Collects data and maintains confidential records and participant database.
  • Will 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.

Benefits

  • Comprehensive benefits
  • Career advancement opportunities
  • Differentials
  • Premiums
  • Bonuses as applicable
  • Recognition programs
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