Data Coordinator

Role Overview

The Data Coordinator provides support to the Clinical Research Coordinator (CRC) and Research Nurse on a daily basis, ensuring all activities are conducted according to company standard operating procedures (SOPs) and all applicable Good Clinical Practice (GCP) and ICH regulations and guidelines.

• Support CRC to meet industry trial data deadlines.
• Obtain source documentation for patients enrolled onto clinical trials.
• Assist CRC 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 CTS.
• Maintain and archive study administrative files.
• Maintain and archive regulatory files.
• Assist in ensuring source document templates are accurate.
• Be assigned special procedural projects to enhance the functioning of the research program.
• Assess adherence to SCRI SOPs, GCP, and ICH regulations throughout the conduct of the clinical trial.

• 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.

Salary range: $24/hr – $27/hr.

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.