Clinical Data Associate I

Responsibilities

• Review and issue queries for CRF data based on automated edit checks, manual reviews, and sponsor requirements
• Perform functional testing of project databases to ensure accuracy
• Ensure project databases align with CRF data and the results of data queries
• Prepare study-specific status reports
• Assist with the setup of data management study files and the archiving of study documentation
• Maintain all necessary documentation to support the integrity of project databases
• Perform all duties according to CTI Standard Operating Procedures (SOPs) and ICH/GCP guidelines

Requirements

• Bachelor’s degree in biological, behavioral, or computer science (or 2 years of clinical research experience)
• 0-2 years of scientific research experience
• Knowledge of ICH/GCP guidelines and applicable regulatory requirements
• Experience with clinical data platforms such as Oracle Clinical, Medidata, OmniComm TrialMaster, or IBM Clinical Development

Preferred Qualifications

• Experience with medical coding
• Experience with database development and programming

Benefits

• Structured mentoring programs and leadership development courses
• Dedicated training department to support professional growth
• Opportunities for ongoing education

About the Company

CTI is a global clinical research organization spanning 60 countries. We are dedicated to advancing medicine by helping develop life-changing treatments for patients with chronic and critical illnesses. We prioritize our people through an award-winning culture and a commitment to professional excellence.