Data Process Associate

Step into the critical role of a Data Process Associate and contribute to the success of clinical trials by ensuring accurate and compliant data management. This role offers you the chance to develop key skills, work alongside experienced professionals, and build a strong foundation for your future in clinical research. If you're detail-focused and driven to support meaningful healthcare advancements, this is your opportunity to grow and make a difference.

What You Will Do:

• Accurately enter and verify clinical data from Case Report Forms (CRFs) into study databases in accordance with established guidelines.
• Perform quality control checks to ensure data accuracy, integrity, and compliance with regulatory requirements.
• Assist with database testing, documentation preparation, and clinical data processing across multiple projects.
• Support User Access Management for Electronic Data Capture (EDC) systems and maintain related documentation.
• Collaborate with project managers and cross-functional teams to ensure timely completion of data management activities.
• Identify process improvement opportunities and contribute to maintaining high-quality standards.
• Perform medical coding activities and other assigned tasks to support successful study completion.

What You Will Gain:

• Gain hands-on experience in clinical data management within a regulated and fast-paced envi