Clinical Trials Source Documents Specialist

Sarah Cannon Research Institute; Nashville (TN); Presencial; USD 42.000 - 62.000; Jornada completa

Descripción de la vacante

Sarah Cannon Research Institute (SCRI) in Nashville, TN is seeking a Source Document Specialist to support the Study Coordinator in daily trial activities. You will ensure compliance with SOPs, GCP and ICH regulations, and help secure accurate source documentation for enrolled patients.

Ideal candidates hold an associate degree (bachelor preferred), at least 2 years in healthcare (oncology preferred), and strong English communication.

Formación

• Health care experience, oncology preferred.
• Knowledge of scientific, medical, and regulatory terms is required.
• GCP and GMP knowledge is beneficial.

Responsabilidades

• Support Study Coordinator to meet industry trial data deadlines.
• Obtain source documentation for patients enrolled in clinical trials.
• Assist with case report form completion as needed.
• Assist with query resolution as needed.
• Obtain medical records including research charts and maintain accountability spreadsheets.
• Collaborate with Tennessee Oncology medical records and Iron Mountain for archives.
• Meet with the project manager regularly and ensure SOPs, GCP, and ICH adherence.

Conocimientos

Health care experience

Clinical trials support

Regulatory terms knowledge

Detail-oriented

Excellent English communication

Educación

Associate Degree

Bachelor Degree preferred

Descripción del empleo

Sarah Cannon Research Institute (SCRI) in Nashville, TN is seeking a Source Document Specialist to support the Study Coordinator in daily trial activities. You will ensure compliance with SOPs, GCP and ICH regulations, and help secure accurate source documentation for enrolled patients.

Ideal candidates hold an associate degree (bachelor preferred), at least 2 years in healthcare (oncology preferred), and strong English communication.