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Clinical Research Coordinator I

Velocity Clinical Research
Velocity Clinical Research
1-3+ years
Not Disclosed
10 March 26, 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

Clinical Research Coordinator I | Entry-Level Clinical Trials | Velocity Clinical Research

Company: Velocity Clinical Research
Job ID: 2026-3383
Job Type: Full-Time (Permanent)
Work Mode: On-site (No Telecommute)
Experience: 1–3+ Years
Location: Not explicitly specified (Site-Based Clinical Role)


Job Overview

Velocity Clinical Research is hiring a Clinical Research Coordinator I (CRC I) to support clinical trial operations, patient management, and regulatory compliance. This is an excellent entry-level opportunity for candidates looking to build a career in clinical research, drug development, and healthcare operations.

As a CRC I, you will be responsible for coordinating clinical studies, ensuring patient safety, managing study documentation, and maintaining compliance with ICH-GCP and regulatory standards.


Key Responsibilities

Clinical Trial Coordination

  • Conduct and manage clinical trials in accordance with study protocols, ICH-GCP, and SOPs

  • Support study start-up, execution, and close-out activities

  • Coordinate subject recruitment, scheduling, and study visits

Patient Safety & Clinical Support

  • Ensure safety and well-being of study participants

  • Perform clinical tasks such as phlebotomy, ECG, drug administration, and lab processing

  • Screen and evaluate potential participants (pre-screening and screening)

Regulatory & Compliance

  • Prepare and submit documents to IRBs and sponsors

  • Ensure compliance with GCP, ICH guidelines, and regulatory requirements

  • Maintain audit-ready documentation and regulatory binders

Data Management & Documentation

  • Enter clinical data into EDC systems and resolve queries

  • Follow Good Documentation Practices (GDP)

  • Maintain confidentiality of patient and sponsor data

Pharmacovigilance & Safety Reporting

  • Monitor and report Adverse Events (AE) and Serious Adverse Events (SAE)

  • Ensure timely escalation and compliance with safety protocols

Stakeholder Coordination

  • Communicate with investigators, sponsors, CROs, and vendors

  • Support cross-functional collaboration for smooth trial execution


Required Skills & Qualifications

Education & Experience

  • Bachelor’s degree + 1 year clinical research experience
    OR

  • Associate’s degree + 2 years experience
    OR

  • High School/Technical degree + 3 years experience

Certifications (If Required)

  • Phlebotomy certification

  • Intramuscular dose administration certification

Technical Skills

  • Knowledge of medical terminology and clinical trial processes

  • Understanding of ICH-GCP, clinical protocols, and regulatory compliance

  • Familiarity with EDC systems and Microsoft Office tools

Core Competencies

  • Strong organizational and multitasking skills

  • Excellent communication and teamwork ability

  • High attention to detail and problem-solving mindset

  • Ability to work in a fast-paced clinical environment

  • Adaptability and willingness to learn


Perks & Benefits

  • Medical, dental, and vision insurance

  • Paid time off and company holidays

  • 401(k) retirement plan with company match

  • Annual performance-based incentive program

  • Career growth opportunities in clinical research and pharma industry

  • Hands-on experience in clinical trials and patient care


Compensation

  • Salary Range: Not disclosed (competitive entry-level clinical research salary)


About the Company

Velocity Clinical Research is a leading integrated clinical research site organization focused on high-quality data generation, patient care, and efficient clinical trial execution. The company partners with sponsors and CROs to accelerate drug development and deliver innovative treatments globally.


Why This Role is Perfect for Beginners

This role is ideal for professionals aiming to start or grow in:

  • Clinical Research & Trial Operations

  • Pharmacovigilance & Drug Safety

  • Regulatory Affairs & Compliance

  • Clinical Data Management

  • Healthcare & Life Sciences Careers


Application Process

Apply through the official Velocity Clinical Research careers portal.


Call to Action

If you want to enter the core of clinical research and drug development, this role is your launchpad.

Get hands-on experience, work on real clinical trials, and build a strong foundation in pharma.
Apply now and kickstart your career in clinical research. 🚀