Hybrid Clinical Research Coordinator, Urology

2200 The Brigham and Women's Hospital, Inc.; Boston (MA); Hybrid; USD 57,859,000 - 63,370,000; Full time

Job summary

The Brigham and Women's Hospital, Inc. is seeking a Clinical Research Coordinator for the Dept. of Urology to enroll patients in cancer studies and manage data collection for multiple protocols.

You will liaise with the clinical team, sponsor, and IRB to ensure communications and reporting are accurate and timely. This role involves data abstraction, regulatory management, and patient coordination, with opportunities to mentor staff and contribute to process improvements in a hybrid work setting

Qualifications

• Bachelor's degree in a related field required.
• 0–1 year experience required.
• Exceptional time management and organization skills.
• Excellent written and verbal communication skills.
• Knowledge of current and developing clinical research trends.
• Strong interpersonal skills and ability to mentor others.
• Ability to identify problems and develop solutions.
• Demonstrated ability to manage multiple projects.

Responsibilities

• Identify changes to SOPs and develop compliant procedures.
• Manage studies within a specialized program.
• Organize and prepare for internal/external audits.
• Participate in recruitment for new hires.
• Mentor junior staff.
• Assist with verification of new study and amendment activation requirements.
• Assist with New Protocol Intake Sheet for regulatory routing.
• Maintain ongoing communication with the clinical team regarding study patients and progress.

Skills

Excellent written and verbal comms

Time management

Organizational skills

Clinical research trends

Interpersonal skills

Problem solving

Multi-project management

Education

Bachelor's degree in related field

Job description

The Brigham and Women's Hospital, Inc. is seeking a Clinical Research Coordinator for the Dept. of Urology to enroll patients in cancer studies and manage data collection for multiple protocols.

You will liaise with the clinical team, sponsor, and IRB to ensure communications and reporting are accurate and timely. This role involves data abstraction, regulatory management, and patient coordination, with opportunities to mentor staff and contribute to process improvements in a hybrid work setting