Senior Clinical Research Coordinator - Data & Protocol Design

2200 The Brigham and Women's Hospital, Inc.; Boston (MA); On-site; USD 56,000 - 82,000; Full time

Job summary

The Brigham and Women's Hospital, Inc. is seeking a clinical research professional to support multiple studies under established policies and protocols.

You will recruit, evaluate, consent patients, collect and organize data, schedule visits, and perform tests such as phlebotomy and EKGs, contributing to data quality and study progress. Responsibilities include input on recruitment strategy, methodology design, statistical analyses, protocol development, and manuscript writing, with emphasis on

Qualifications

• Education: Bachelor's Degree related field required or Graduate Diploma preferred.
• Experience: 3–5 years post-bachelor's research experience.
• Skills: high computer literacy, analytical abilities, data management proficiency.

Responsibilities

• Independently determines suitability of study subjects.
• Develops and implements recruitment strategies.
• Participates in design of research methodology.
• Plans, performs, and designs statistical analyses.
• Recommends protocol changes, writes protocols, and contributes to manuscripts.
• Independently performs specialized projects.

Skills

Data management

Analytical skills

Time management

Written and verbal communication

Team collaboration

Education

Bachelor's Degree related field

Graduate Diploma related field

Tools

Data management systems

Job description

The Brigham and Women's Hospital, Inc. is seeking a clinical research professional to support multiple studies under established policies and protocols.

You will recruit, evaluate, consent patients, collect and organize data, schedule visits, and perform tests such as phlebotomy and EKGs, contributing to data quality and study progress. Responsibilities include input on recruitment strategy, methodology design, statistical analyses, protocol development, and manuscript writing, with emphasis on