Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Manager, Edc

Velocity Clinical Research
Velocity Clinical Research
4-6 years
Not Disclosed
10 March 20, 2026
Job Description
Job Type: Full Time Education: 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

Manager, EDC

Company: Velocity Clinical Research
Location: On-site
Job Type: Full-Time
Experience: 4–6 Years (with 2–3 Years leadership preferred)
Qualification: Bachelor’s / Associate Degree (preferred)


Job Overview

This role focuses on managing Electronic Data Capture (EDC) systems and ensuring high-quality clinical trial data. You will support clinical teams in data entry, validation, and query resolution while ensuring compliance with GCP, FDA, and sponsor requirements.


Key Responsibilities

EDC System Management

  • Configure and manage EDC systems for clinical trials

  • Support site staff with data entry and validation processes

  • Identify and resolve system issues with IT/vendors

Data Quality & Validation

  • Monitor data discrepancies and perform data cleaning

  • Ensure accuracy, completeness, and consistency of clinical data

  • Manage query resolution and validation checks

Regulatory Compliance

  • Ensure adherence to GCP, FDA, and sponsor guidelines

  • Maintain data integrity and audit readiness

Collaboration & Coordination

  • Work with clinical teams, sponsors, and IT teams

  • Optimize data workflows and reporting processes

  • Support secure and efficient data collection systems


Required Skills

Strong understanding of clinical trial data management

Knowledge of GCP and regulatory requirements

Analytical thinking and attention to detail

Problem-solving and system troubleshooting

Ability to work in fast-paced environments


Preferred Skills

Supervisory or team management experience

Experience with EDC systems and data workflows

Strong coordination and communication skills