Breast Oncology Clinical Trials Coordinator

Dana-Farber Cancer Institute; Boston (MA); On-site; USD 48,000 - 54,000; Full time

Job summary

The Clinical Research Coordinator (CRC) will work within the Breast Oncology clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager.

The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials.

Qualifications

• Bachelor’s Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience required.
• 0-1 years of experience in medical or scientific research setting preferred.
• Must adhere to Good Clinical Practice and institutional guidelines.

Responsibilities

• Oversee data collection and management of patient clinical information for trials.
• Ensure timely trial assessments per protocol and sample shipping as required.
• Maintain regulatory and study binders; assist with IRB submissions as needed.
• Register participants in the clinical trials management system ONCORE and coordinate site activities.
• Prepare for internal and external audits and monitor visits.

Skills

Organization

Interpersonal skills

Attention to detail

Time management

Discretion

Microsoft Office

Education

Bachelor's Degree

Job description

The Clinical Research Coordinator (CRC) will work within the Breast Oncology clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager.

The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials.