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# Data Coordinator (EDC)

- **Company:** Alcanza Clinical Research
- **Location:** Decatur, GA, United States
- **Contract:** Permanent contract
- **Skills:** Software Applications, Clinical Data Repository, Microsoft Software, Web Applications, Information Technology, Intercompany Hub
- **Published:** October 13, 2026
- **Apply:** https://www.thejobnetwork.com/job/259557d2-5fa1-469f-abf4-b308156bec0e/data-coordinator-edc

## About the Role

Skills, Knowledge and ExpertiseMinimum Qualifications: High School diploma or equivalent and a minimum of 1 year of clinical data entry experience, or an equivalent combination of education and experience., * Proficiency with computer applications such as Microsoft applications, email, and web applications, and the ability to type proficiently (40+ wpm);

 * Strong organizational skills and attention to detail.
 * Well-developed written and verbal communication skills.
 * Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
 * Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
 * Must be professional, respectful of others, self-motivated, and have a strong work ethic.
 * Must possess a high degree of integrity and dependability.
 * Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

## Description

The Data Entry Coordinator works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.
Key ResponsibilitiesEssential Job Duties:

In collaboration with other members of the clinical research site teamwork to ensure the entry of clinical visit data in EDC and other clinical data software/systems. Responsibilities may include but are not limited to:

 * Managing data entry into computer systems for clinical trials, including entering patient data into eDC and other software
 * Reviewing patient charts and other medical records to ensure data is entered in a timely manner in accordance with eCRF guidelines and protocol requirements
 * Reporting any irregularities or problems with a study to the appropriate parties
 * Supporting other clinical research-related activities
 * Ensuring compliance with SOPs, regulations, ICF documentation, and GCP/GDP guidelines
 * Maintaining confidentiality of patients, customers, and company information, and performing other related activities as assigned.