Clinical Trials Coordinator — Onsite Research

Brigham and Women's Hospital; Massachusetts; On-site; USD 29,000 - 40,000; Full time

Job summary

The Brigham and Women's Hospital, Inc. is seeking a Clinical Research Support role to assist with ongoing clinical studies across departments, including recruitment, data collection, and coordinating patient visits.

Ideal candidates have a Science degree, are comfortable with regulatory processes, and can work onsite at Mass General Brigham facilities. Overnight and weekend shifts may be required, with a 40-hour work week.

Qualifications

• Bachelor's Degree in Science required.
• EMT preferred.
• Bilingual in Spanish and English preferred.

Responsibilities

• Reviews proposals for compliance with sponsor and organizational guidelines; verify all sponsor requirements are met.
• Recruiting patients for clinical trials, conducts phone calls.
• 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.

Skills

Attention to detail

Interpersonal skills

Communication skills

Computer literacy

Clinical research protocols

Education

Bachelor's degree in Science

Job description

The Brigham and Women's Hospital, Inc. is seeking a Clinical Research Support role to assist with ongoing clinical studies across departments, including recruitment, data collection, and coordinating patient visits.

Ideal candidates have a Science degree, are comfortable with regulatory processes, and can work onsite at Mass General Brigham facilities. Overnight and weekend shifts may be required, with a 40-hour work week.