Clinical Trials Source Document Specialist – Cancer Care

McKesson; Nashville (TN); On-site; USD 42,000 - 62,000; Full time

Job summary

McKesson’s Sarah Cannon Research Institute (SCRI) in Nashville seeks a Source Document Specialist to support the Study Coordinator and ensure regulatory adherence in clinical trials. The role emphasizes data integrity, document management, and cross-team collaboration within oncology trial operations.

Required Associate degree; bachelor’s degree preferred. Healthcare experience and knowledge of GCP and GMP are highly valued; excellent English communication skills are essential.

Qualifications

• Associate degree required; bachelor’s degree preferred.

Responsibilities

• Provide daily support to the Study Coordinator.
• Ensure activities follow SOPs, GCP and ICH guidelines.
• Support meeting industry trial data deadlines.
• Obtain source documentation for patients enrolled in trials.
• Assist with case report form completion as needed.
• Assist with query resolution as needed.
• Obtain medical records and research charts.
• Create and maintain spreadsheets for record accountability.
• Maintain study administrative files.
• Coordinate with Tennessee Oncology medical records to ensure accountability.
• Coordinate with Iron Mountain to locate archived records.
• Meet with the project manager regularly.
• Assess adherence to SOPs and GCP/ICH regulations.

Skills

Attention to detail

English communication

Education

Associate Degree

Bachelor Degree preferred

Job description

McKesson’s Sarah Cannon Research Institute (SCRI) in Nashville seeks a Source Document Specialist to support the Study Coordinator and ensure regulatory adherence in clinical trials. The role emphasizes data integrity, document management, and cross-team collaboration within oncology trial operations.

Required Associate degree; bachelor’s degree preferred. Healthcare experience and knowledge of GCP and GMP are highly valued; excellent English communication skills are essential.