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Coordinator, Edc

Velocity Clinical Research
Velocity Clinical Research
1-2 years
Not Disclosed
10 March 20, 2026
Job Description
Job Type: Full Time Education: B.E./B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Coordinator, EDC

Company: Velocity Clinical Research
Location: On-site
Job Type: Full-Time
Experience: 1–2 Years
Qualification: Bachelor’s / Technical Degree (preferred)


Job Overview

This is an entry-level to mid-level role focused on supporting Electronic Data Capture (EDC) systems in clinical trials. You will assist in data entry, validation, and query resolution while ensuring compliance with GCP, FDA, and sponsor requirements.


Key Responsibilities

EDC Support & Data Entry

  • Assist site staff with accurate data entry in EDC systems

  • Support query resolution and validation checks

  • Ensure timely and accurate data updates

Data Quality & Cleaning

  • Monitor discrepancies in clinical data

  • Perform data cleaning and validation activities

  • Maintain data accuracy and consistency

Regulatory Compliance

  • Follow GCP, FDA, and sponsor-specific guidelines

  • Ensure proper documentation and audit readiness

System & Workflow Coordination

  • Work with clinical teams, sponsors, and IT teams

  • Support optimization of data collection workflows

  • Escalate system issues to vendors or IT teams


Required Skills

Basic understanding of clinical trial data collection

Knowledge of GCP and regulatory requirements (preferred)

Attention to detail and organizational skills

Analytical thinking and problem-solving

Ability to work independently and in teams


Preferred Skills

Experience with EDC systems

Exposure to clinical research or healthcare settings

Understanding of IRB and FDA processes