Clinical Research Coordinator II – Onsite Trials

2200 The Brigham and Women's Hospital, Inc.

Boston (MA)

On-site

USD 51,000 - 82,000

Full time

5 days ago
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Job summary

The Brigham and Women's Hospital, Inc. is seeking a Clinical Research Assistant to support multiple clinical studies at the Mass General Brigham system. You will assist with study protocols, recruit patients, collect data, and coordinate IRB submissions and communications with collaborators.

Under supervision, you will manage screening, scheduling, data entry, and budgeting tasks to ensure accurate study records and compliant operations across multiple sites.

Qualifications

  • Requires a Bachelor's Degree in a science field.
  • At least 1 year of research experience post-bachelor's.

Responsibilities

  • Assists with clinical research studies per guidelines and protocols.
  • Screen for eligibility, recruit and evaluate potential study patients.
  • Conduct telephone interviews or schedule in-person study visits and screenings.
  • May perform clinical tests if certified and as needed.
  • Set up lab testing, shipping, etc. with colleagues in research labs.
  • Collect data and maintain the patient information database for several studies.
  • Prepare materials and answer inquiries regarding study protocol.
  • Coordinate with sponsor companies, CRAs, central labs, and testing facilities.
  • Oversee study budgets and patient reimbursements.
  • Prepare and submit all IRB documents: applications, amendments, annual reviews, and adverse events.

Skills

Clinical research support
Data collection

Education

Bachelor's Degree
Science

Job description

The Brigham and Women's Hospital, Inc. is seeking a Clinical Research Assistant to support multiple clinical studies at the Mass General Brigham system. You will assist with study protocols, recruit patients, collect data, and coordinate IRB submissions and communications with collaborators.

Under supervision, you will manage screening, scheduling, data entry, and budgeting tasks to ensure accurate study records and compliant operations across multiple sites.

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