job title: Coordinator, EDC(Velocity clinical research)

Roles and Responsibilities

Duties/Responsibilities:

· Support clinical research site staff with accurate data entry, query resolution, and validation checks to ensure data quality.

· Ensure data management processes adhere to Good Clinical Practice (GCP), FDA, and sponsor-specific regulations.

· Monitor data discrepancies, perform data cleaning activities

· Work closely with clinical research teams, sponsors, and IT teams to optimize data collection, reporting, and security.

· Identify and resolve EDC system issues, escalating as necessary to vendors or IT teams.

· Other duties as assigned

Qualifications

Required Skills/Abilities:

· Strong understanding of clinical trial data collection, GCP guidelines, and regulatory requirements.

· Excellent analytical skills and attention to detail to ensure data accuracy and compliance.

· Ability to work independently and collaboratively in a fast-paced clinical research setting.

Education and Experience:

· Highschool Diploma required, Bachelor's degree or Technical Degree in life sciences, healthcare, or related field preferred.

· Strong attention to detail, organizational skills, and ability to follow protocols. Familiarity with research regulations (GCP, IRB, FDA) is a plus.

· Experience: 1-2 years of experience in clinical research, healthcare, or laboratory settings.