Clinical Research Job at Velocity Clinical Research
Velocity Clinical Research is seeking a Clinical Research Coordinator I to join its Clinical Operations team. This temporary, on-site opportunity is ideal for professionals passionate about clinical research, patient care, and regulatory compliance. This Clinical Research Job focuses on conducting and managing clinical trials in accordance with study protocols, ICH-GCP guidelines, and company SOPs while ensuring high-quality data and patient safety.
About the Company:
Velocity Clinical Research is an owned and integrated research site organization committed to excellence in patient care and high-quality clinical data generation. The organization focuses on accelerating clinical trials by enrolling patients efficiently while maintaining exemplary standards of care.
Velocity invests in employee growth, supports career advancement, and rewards high performance, making it an ideal workplace for both new professionals and experienced clinical research experts.
Job Details:
- Job Title: Clinical Research Coordinator I
- Category: Clinical Operations
- Job ID: 2026-3281
- Position Type: Temporary
- Telecommute: No
- Industry: Clinical Research
Educational Requirements:
- Bachelor’s degree with 1 year of relevant experience in the life science industry OR
- Associate’s degree with 2 years of relevant experience in the life science industry OR
- High School Graduate and/or technical degree with a minimum of 3 years relevant experience in the life science industry
Required Certifications (if applicable by state law):
- Phlebotomy certification
- Intramuscular dose administration and preparation certification
Key Responsibilities:
- As a Clinical Research Coordinator, you should conduct and manage clinical trials in accordance with study protocol, GCP, ICH Guidelines, and company SOPs
- Coordinate study start-up, vendor management, subject recruitment, scheduling, and regulatory document collection
- Conduct subject visits and ensure timely data entry and query resolution in this Clinical Research Job
- Manage and report adverse events, serious adverse events, and protocol deviations
- Implement protocol amendments and provide close-out reports
- In this Clinical Research Job, at Velocity Clinical Research, you should maintain patient confidentiality and protected health information
- Ensure patient safety and compliance with regulatory standards
- Create, collect, and submit regulatory documents to Sponsors and IRBs
- Evaluate potential subjects through phone and in-person pre-screens
- Execute recruitment strategies defined by the Clinical Research Team
- Perform clinical duties such as drug preparation and administration, fibroscan, phlebotomy, ECG, and lab processing in this Clinical Research Job
- Maintain good documentation practices and ensure accurate data transfer
Skills Required:
- Knowledge of medical terminology
- Proficiency with computers and Microsoft Office software
- Strong verbal, written, and organizational skills
- Strong interpersonal and communication skills
- Ability to work in a fast-paced environment
- Ability to multitask and prioritize effectively
- Detail-oriented with strong problem-solving skills
- Ability to work independently and as a team player
- Flexibility to adapt to rapidly changing schedules
- Professionalism and accountability
Physical Requirements:
- Ability to sit or stand for long periods
- Limited walking and lifting up to 30 pounds
- Ability to travel locally and nationally
- Ability to communicate in person and by telephone
Benefits of the Clinical Research Job:
- Medical, dental, and vision insurance
- Paid time off and company holidays
- 401(k) retirement plan with company match
- Annual incentive program
- Career advancement opportunities
- Supportive and performance-driven work culture
