Clinical Research Coordinator - INSPIRE Lab

Mass General BrighamCambridge, MA
$21 - $29Onsite

About The Position

The mission of the Spaulding Rehabilitation Hospital INSPIRE Lab is to enable people to regain functional independence after paralysis. To achieve this mission, our interdisciplinary team researches novel technologies that integrate rehabilitation, physiology, and engineering principles to promote the restoration of limb movements and function in persons with catastrophic injuries to their nervous systems. Clinical Research Coordinators play an essential role in our mission. The CRC works within the INSPIRE Lab, located at Spaulding Rehabilitation Hospital, Cambridge. The CRC helps with research experiments, data collection, data analysis, regulatory documentation, study recruitment, and other technical duties. Seeking candidates for a start date in early summer 2026.

Requirements

  • Bachelor's Degree Related Field of Study required
  • Some relevant research project work 0-1 year preferred
  • Careful attention to detail and good organizational skills.
  • Ability to follow directions.
  • Good interpersonal and communication skills.
  • Computer literacy.
  • Working knowledge of clinical research protocols.
  • Ability to demonstrate respect and professionalism for subjects' rights and individual needs.

Nice To Haves

  • Candidates who are in the process of completing their bachelor's degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification.

Responsibilities

  • Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
  • Recruiting patients for clinical trials and conducting phone interviews.
  • Verifies the accuracy of study forms and updates them per protocol.
  • Prepares data for analysis and data entry.
  • Documents patient visits and procedures.
  • Assists with regulatory binders and QA/QC Procedures.
  • Assists with interviewing study subjects.
  • Assists with study regulator submissions.
  • Provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; and maintaining and updating data generated by the study.

Benefits

  • comprehensive benefits
  • career advancement opportunities
  • differentials
  • premiums
  • bonuses
  • recognition programs
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