Clinical Research Coordinator Job | Velocity Clinical Research Careers
Looking for a rewarding clinical research coordinator job that blends data accuracy, compliance, and patient care? Velocity Clinical Research, Inc. offers a dynamic opportunity for professionals eager to grow in the field of clinical research jobs. As a clinical research coordinator, you’ll contribute to groundbreaking studies that shape the future of healthcare. This role is ideal for those seeking to advance their career in a fast-paced, data-driven healthcare job environment.
- Job Position: Coordinator, EDC – Quality Control
- Job ID: 2025-3191
About the Company:
Velocity Clinical Research, Inc. is a leading global organization committed to advancing medical innovation through world-class clinical research jobs. With a network of state-of-the-art research sites and expert teams, Velocity specializes in conducting high-quality trials that accelerate drug and vaccine development while maintaining strict standards of safety and compliance.
Qualifications:
Education and Experience:
- Preferred Education: Bachelor’s degree in healthcare or a related field.
- Experience: 1–2 years of experience in clinical research, healthcare, or laboratory settings.
- Familiarity with GCP, IRB, and FDA regulations is a plus.
Clinical Research Coordinator Job Description:
The Clinical Research Coordinator will be responsible for managing and supporting clinical research teams in accurate data entry, validation, and adherence to regulatory and sponsor requirements. This clinical research coordinator job focuses on optimizing electronic data workflows, ensuring data integrity, and maintaining compliance with Good Clinical Practice (GCP), FDA, and sponsor-specific regulations.
Clinical Research Coordinator Job – Key Responsibilities:
- Support clinical research site staff with precise data entry, query resolution, and validation checks to ensure top-quality data.
- Monitor data discrepancies and perform data cleaning activities to maintain data integrity.
- Ensure all data management processes comply with GCP, FDA, and sponsor requirements.
- Collaborate with clinical research teams, sponsors, and IT departments to optimize data collection, reporting, and data security.
- Identify, troubleshoot, and escalate electronic data capture (EDC) system issues to vendors or IT support teams.
- Perform other related duties as assigned by management.
Required Skills and Abilities:
- Strong understanding of clinical trial data collection and regulatory guidelines.
- Excellent analytical skills and attention to detail for data accuracy and compliance.
- Ability to work independently and collaboratively in a fast-paced research environment.
