Data Coordinator

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

Data Coordinator

Provides support to Study Coordinator on a daily basis, ensures all activities are conducted according to company SOPs and all applicable GCP and ICH regulations and guidelines.

Responsibilities

• Support the Study Coordinator to meet industry trial data deadlines.
• Obtain source documentation for patients enrolled into clinical trial.
• Assist the Study Coordinator with case report form completion and query resolution.
• Assist in Serious Adverse Event (SAE) reporting and tracking.
• Create and maintain patient visit tracking spreadsheets for the Study Coordinator.
• Maintain and archive study administrative files.
• Be assigned special procedural projects to enhance the functioning of Drug Development Data Operations.
• Assess adherence to SCRI SOPs, GCP and ICH regulations and guidelines throughout the conduct of the clinical trial.

Qualifications

• Knowledge of scientific, medical, and regulatory terms.
• Knowledge of GCP and Good Manufacturing Practice (GMP).
• Detail-oriented.
• Excellent English written and oral skills.
• Bachelor’s Degree preferred.
• Healthcare experience, clinical trials support, or pharmaceutical industry experience preferred.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.