Clinical Data Coordinator - Trials Support & Compliance

McKesson Corporation; Nashville (TN); On-site; USD 40,000 - 60,000; Full time

Job summary

McKesson Corporation is seeking a Data Coordinator in Nashville, Tennessee. The role involves supporting the Study Coordinator in meeting clinical trial data deadlines and ensuring adherence to regulatory guidelines.

Ideal candidates will be detail-oriented and possess knowledge of scientific and medical terms, with a preference for those holding a Bachelor's Degree and having experience in healthcare or clinical trials.

Qualifications

• Knowledge of GCP and Good Manufacturing Practice (GMP).
• Healthcare experience, clinical trials support, or pharmaceutical industry experience preferred.

Responsibilities

• Support the Study Coordinator to meet industry trial data deadlines.
• Obtain source documentation for patients enrolled into clinical trial.
• Assist in Serious Adverse Event (SAE) reporting and tracking.
• Maintain and archive study administrative files.

Skills

Knowledge of scientific, medical, and regulatory terms

Detail-oriented

Excellent English written and oral skills

Education

Bachelor’s Degree preferred

Job description

McKesson Corporation is seeking a Data Coordinator in Nashville, Tennessee. The role involves supporting the Study Coordinator in meeting clinical trial data deadlines and ensuring adherence to regulatory guidelines.

Ideal candidates will be detail-oriented and possess knowledge of scientific and medical terms, with a preference for those holding a Bachelor's Degree and having experience in healthcare or clinical trials.