Job Details

A company is looking for a Clinical Research Data Specialist I.

Key Responsibilities

• Extract and enter clinical and research data from electronic medical records into data capture systems for oncology clinical trials
• Track research subjects' appointments and ensure compliance with data entry requirements
• Manage adverse event data and independently handle tumor response and quality of life assessments data entry

Required Qualifications

• Bachelor's Degree in a related field required
• 1-2 years of research-related experience preferred
• Working knowledge of clinical research protocols
• Ability to recognize compliance and data integrity issues
• Experience with data management quality control steps