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Clinical Research Assistant

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Boston Children's Hospital

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Location:
United States , Boston

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Category:
Research and Development

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Contract Type:
Not provided

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Salary:

41246.40 - 61339.20 USD / Year
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Job Description:

At Boston Children’s Hospital, the quality of our care – and our inclusive hospital working environment – lies in the diversity of our people. With patients from local communities and 160 countries around the world, we’re committed to reflecting the spectrum of their cultures, while opening doors of opportunity for our team. Here, different talents pursue common goals. Voices are heard and ideas are shared. Join us, and discover how your unique contributions can change lives. Yours included.

Job Responsibility:

  • Coordinates daily activities and operations of clinical research studies
  • Screens and enrolls patients
  • Monitors protocol implementation
  • Completes required forms and reporting results
  • Conducts regulatory submissions
  • Conducts data collection activities
  • May prepare analytical reports on study results
  • Follows established clinical study standards and procedures
  • Maintain open communication with team members to ensure proper study progress
  • Consents and enrolls patients for research studies by providing detailed information on the Research Study to patients and families
  • Understands and adheres to all policies and procedures
  • Responds to all inquiries
  • Obtains informed consent and enrolls patients in research studies
  • Reviews clinical information to identify patients meeting study inclusion criteria
  • Serves as liaison to the families/patients in the research studies, conducted at both on site and off-site locations
  • Guides and advises patients and families throughout each phase of the study
  • Coordinates follow up visits as necessary
  • Acts as a resource to study participants
  • Troubleshoots resolution of any issues that may arise throughout the study
  • Coordinates and prepares documentation needed for Institutional Review Board (IRB) on submissions, for PI approval
  • Tracks progress from submission to approval
  • Assists in developing supportive study documents such as informed consent forms, monitoring templates, study subject tracking tools, monitoring forms, study manuals, and training materials
  • Assists with the tracking and compilation of enrollment information
  • May assist with preparation of manuscripts and reports to be submitted to academic journals
  • May help train and orient newly hired study personnel
  • Coordinates activities with various departments to ensure correct testing/processing and sends clear instructions to each study
  • Monitors and reviews data collection and data entry
  • Monitors and reviews informed consent procedures ensuring consistency of application for each study

Requirements:

  • Bachelor’s degree in a science field required
  • 0-1 years of experience required
What we offer:
  • Flexible schedules
  • Affordable health insurance
  • Vision insurance
  • Dental insurance
  • Child care subsidies
  • Student loan subsidies
  • Generous levels of time off
  • 403(b) Retirement Savings plan
  • Pension
  • Tuition Reimbursement
  • Certain License and Certification Reimbursement
  • Cell phone plan discounts
  • Discounted rates on T-passes

Additional Information:

Job Posted:
May 16, 2026

Employment Type:
Fulltime
Work Type:
Hybrid work
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