Velocity CRO is inviting applications for the position of EDC Coordinator (Electronic Data Capture Coordinator) to support clinical research data management and quality control activities. This opportunity is ideal for candidates with 1โ2 years of clinical research experience and knowledge of GCP guidelines, FDA regulations, and clinical trial data systems.
The EDC Coordinator role in a CRO environment focuses on maintaining clinical trial data accuracy, supporting site teams with electronic data entry, resolving queries, and ensuring regulatory compliance during clinical research studies.
Professionals interested in clinical research jobs, clinical data management roles, and EDC system management will find this opportunity highly valuable for career growth in the CRO and clinical trials industry.
Job Details
Company: Velocity CRO
Position: EDC Coordinator
Category: Quality Control / Clinical Data Management
Employment Type: Full-Time
Mode: On-site
Experience Required: 1โ2 Years
Industry: Clinical Research / CRO / Data Management
Key Responsibilities
The EDC Coordinator will perform several clinical data management and quality assurance responsibilities, including:
โข Support clinical research site staff with accurate clinical trial data entry into EDC systems.
โข Review and resolve data queries to maintain high-quality clinical trial datasets.
โข Conduct data validation checks and discrepancy management.
โข Perform data cleaning activities to ensure clinical trial database integrity.
โข Ensure all processes comply with Good Clinical Practice (GCP), FDA guidelines, and sponsor requirements.
โข Collaborate with clinical research teams, sponsors, and IT teams to optimize electronic data workflows.
โข Identify and troubleshoot EDC system issues, escalating technical concerns to vendors or IT teams when needed.
โข Support secure data collection, reporting, and regulatory compliance within the clinical trial framework.
Qualifications
Candidates applying for the Velocity CRO EDC Coordinator job should meet the following criteria:
Educational Qualification
โข Bachelorโs Degree or Technical Degree in Life Sciences, Pharmacy, Healthcare, or related field (preferred)
โข High School Diploma minimum requirement
Experience
โข 1โ2 years experience in clinical research, healthcare, or laboratory environments
Skills Required
โข Strong understanding of clinical trial data collection and EDC systems
โข Knowledge of GCP, IRB, and FDA regulations
โข Excellent analytical and data validation skills
โข High attention to detail and documentation accuracy
โข Ability to work independently and in collaborative clinical research teams
Benefits of Working with Velocity CRO
โข Exposure to global clinical research operations
โข Hands-on experience with Electronic Data Capture (EDC) systems
โข Opportunity to work with clinical trial sponsors and research teams
โข Career growth in clinical data management and CRO industry
โข Experience in regulatory-compliant clinical research workflows
How to Apply
