Clinical Trials Coordinator — Patient-Focused Research

Brigham and Women's Hospital; Boston (MA); Sur place; USD 33 000 - 54 000; Plein temps

Résumé du poste

The Brigham and Women's Hospital, Inc. is seeking a clinical research support professional to assist with multiple studies under supervision.

You will recruit and assess potential participants, collect and organize data, and help manage study documentation and communications with sponsors and labs. Responsibilities include scheduling visits, preparing IRB submissions, and ensuring compliance with study protocols while coordinating with investigators and clinical staff.

Qualifications

• Bachelor's Degree required.
• 1-2 years of post-bachelor's research experience preferred.

Responsabilités

• Assist with clinical research studies per protocol and study guidelines.
• Screen for eligibility, recruit and evaluate potential study patients and schedule visits.
• Collect, organize, and maintain patient data and study documents.
• Prepare IRB submissions, amendments, and annual reviews as needed.
• Coordinate with sponsors, CRAs, labs, and study personnel.

Connaissances

Independent work

Team player

Computer literacy

Analytical skills

Data management

Problem solving

Formation

Bachelor's Degree

Description du poste

The Brigham and Women's Hospital, Inc. is seeking a clinical research support professional to assist with multiple studies under supervision.

You will recruit and assess potential participants, collect and organize data, and help manage study documentation and communications with sponsors and labs. Responsibilities include scheduling visits, preparing IRB submissions, and ensuring compliance with study protocols while coordinating with investigators and clinical staff.