Clinical Research Coordinator I | Entry-Level Clinical Trials | Velocity Clinical Research
Company: Velocity Clinical Research
Job ID: 2026-3366
Job Type: Full-Time (Permanent)
Work Mode: On-site (No Telecommute)
Experience: 1–3+ Years
Location: Not specified (Site-Based Role)
Job Overview
Velocity Clinical Research is looking for a Clinical Research Coordinator I (CRC I) to support the execution of clinical trials, patient management, and regulatory compliance activities.
This is a strong entry-level opportunity to build expertise in clinical research operations, pharmacovigilance, and drug development processes, working directly on live clinical studies.
You will be responsible for coordinating trials, ensuring patient safety, accurate data collection, and adherence to ICH-GCP guidelines, making you a key contributor in bringing new therapies to market.
Key Responsibilities
Clinical Trial Operations
Conduct and manage clinical trials as per protocols, ICH-GCP, and SOPs
Support study lifecycle: start-up, execution, and close-out
Coordinate subject recruitment, scheduling, and study visits
Patient Care & Safety
Ensure safety and well-being of trial participants
Perform clinical procedures like phlebotomy, ECG, drug administration, lab processing
Conduct pre-screening and screening of study subjects
Regulatory & Compliance
Prepare and submit regulatory documents to IRBs and sponsors
Ensure compliance with GCP, ICH guidelines, and protocol requirements
Maintain audit-ready documentation and regulatory binders
Data Management & Documentation
Enter and manage data in EDC systems
Follow Good Documentation Practices (GDP)
Resolve data queries and ensure data accuracy
Pharmacovigilance & Safety Reporting
Monitor and report Adverse Events (AE) and Serious Adverse Events (SAE)
Ensure compliance with safety reporting timelines
Stakeholder Coordination
Communicate with investigators, CROs, sponsors, and vendors
Support cross-functional coordination for smooth trial execution
Required Skills & Qualifications
Education & Experience
Bachelor’s degree + 1 year experience
OR
Associate’s degree + 2 years experience
OR
3+ years relevant experience in clinical research
Certifications (If Applicable)
Phlebotomy certification
Intramuscular injection 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 MS Office tools
Core Competencies
Strong organizational and multitasking skills
Effective communication and teamwork
Attention to detail and compliance mindset
Ability to work in fast-paced clinical environments
Problem-solving and adaptability
Perks & Benefits
Medical, dental, and vision insurance
Paid time off and company holidays
401(k) retirement plan with company match
Annual performance-based incentives
Career growth in clinical research and pharma industry
Hands-on exposure to clinical trials and drug development
Compensation
Salary Range: Not disclosed (competitive for entry-level clinical research roles)
About the Company
Velocity Clinical Research is a leading integrated clinical research site network specializing in high-quality data generation, patient-centric trials, and efficient clinical operations. The company collaborates with sponsors and CROs to accelerate drug development and global clinical studies.
Why This Role is a Smart Entry Move
This role is ideal if you want to break into:
Clinical Research & Trial Coordination
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’re serious about entering the clinical research industry and working on real drug development projects, this is your starting point.
Learn fast. Work on real trials. Build a strong pharma career foundation.
Apply now and step into clinical research. 🚀
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