Clinical Research Coordinator I — Trial Operations & Data

Brigham and Women's Hospital, Inc.; Boston (MA); On-site; USD 29,000 - 40,000; Full time

Job summary

Brigham and Women's Hospital, Inc. in Boston invites applications for a Clinical Research Coordinator I to support a portfolio of multidisciplinary clinical trials within the Radiation Oncology program.

You will assist the PI and study team with patient recruitment, consent, data collection, scheduling, and basic clinical tests, ensuring adherence to protocol and regulatory requirements. Qualifications include a Bachelor's degree or equivalent, 0–1 year of relevant experience, and strong

Qualifications

• Bachelor's degree in related field required.
• Experience in lieu of degree accepted.
• 0–1 year of relevant research project experience preferred.

Responsibilities

• Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
• Recruiting patients for clinical trials and conducting phone interviews.
• 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

Follow directions

Interpersonal skills

Computer literacy

Clinical research protocols

Subject rights respect

Education

Bachelor's Degree in Related Field

Job description

Brigham and Women's Hospital, Inc. in Boston invites applications for a Clinical Research Coordinator I to support a portfolio of multidisciplinary clinical trials within the Radiation Oncology program.

You will assist the PI and study team with patient recruitment, consent, data collection, scheduling, and basic clinical tests, ensuring adherence to protocol and regulatory requirements. Qualifications include a Bachelor's degree or equivalent, 0–1 year of relevant experience, and strong