Data Coordinator

About the role

The Data Coordinator provides support to the Study Coordinator 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.

Responsibilities

• You will support the Study Coordinator to meet industry trial data deadlines
• You will obtain source documentation for patients enrolled into clinical trials
• You will assist the Study Coordinator with case report form completion and query resolution
• You will assist in Serious Adverse Event (SAE) reporting and tracking
• You will create and maintain patient visit tracking spreadsheets for the Study Coordinator
• You will maintain and archive study administrative files
• You will be assigned special procedural projects to enhance the functioning of Drug Development Data Operations
• Throughout the conduct of the clinical trial, you will assess adherence to SCRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines

Requirements

• Knowledge of scientific, medical, and regulatory terms
• Knowledge of GCP and Good Manufacturing Practice (GMP)
• Detail-oriented
• Excellent English written and oral skills

Qualifications

• Bachelor Degree preferred
• Healthcare experience, Clinical trials support, or pharmaceutical industry experience preferred

Skills

• Strong organizational and time management skills
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office Suite

Benefits

We not only care about the wellbeing of our patients, customers and the communities we serve — we care about you. That’s why we provide our employees with a comprehensive support system for all aspects of Your Care: physical, emotional, financial and social.