Clinical Research Jobs at Velocity
Velocity Clinical Research is hiring a Clinical Research Coordinator II (CRC II) to manage multiple clinical trials from study start-up through close-out. This part-time position (less than 30 hours/week) is ideal for experienced clinical research professionals who are passionate about patient care, data integrity, and regulatory compliance. The candidate getting hired for the Clinical Research Jobs at Velocity plays a critical part in ensuring high-quality clinical trial execution in accordance with GCP, ICH guidelines, and SOPs.
Job Details:
- Job Title: Clinical Research Coordinator II
- Job ID: 2025-3246
- Category: Clinical Operations
- Employment Type: Part-Time (Less than 30 Hours)
- Work Location: On-site (No Telecommute)
- Industry: Clinical Research / Life Sciences
- Compensation: $30.00 – $36.00 per hour (based on experience, education, and location)
About the Company:
Velocity Clinical Research is an integrated research site organization dedicated to advancing innovative medical treatments through high-quality clinical trials. The company is known for its strong commitment to patient-centered care, data excellence, and operational efficiency. Velocity invests in employee development and fosters a collaborative environment where professionals can grow their clinical research careers while making a meaningful impact on patient health.
Educational Requirements for Clinical Research Jobs:
- Bachelor’s degree with 2 years of relevant life science experience OR
- Associate’s degree with 4 years of relevant life science experience OR
- High School diploma / technical degree with 6 years of relevant life science experience AND
- Minimum 1 year of Clinical Research Coordinator experience
Key Responsibilities:
- Conduct and manage clinical trials in compliance with study protocols, GCP, ICH, and SOPs in this Clinical Research Coordinator Role.
- Coordinate study start-up, subject recruitment, vendor management, and close-out activities
- Schedule study visits and conduct subject pre-screening (phone and in-person)
- Collect, review, and maintain regulatory and source documents
- Ensure accurate and timely data entry and query resolution
- As a Clinical Research Coordinator, you have to manage and report adverse events, serious adverse events, and protocol deviations
- Implement protocol amendments and ensure staff training and delegation
- Prepare and submit regulatory documents to Sponsors and IRBs
- Maintain confidentiality of patient and sponsor information
- Perform clinical procedures such as phlebotomy, ECG, drug administration, lab processing, and fibroscan
- Support quality control activities and monitoring visits
- Collaborate with cross-functional clinical research teams
Skills Required for Clinical Research Jobs:
- Strong knowledge of medical terminology and clinical research processes
- Understanding of GCP, ICH guidelines, and regulatory requirements
- Proficiency in Microsoft Office and clinical data systems
- Excellent verbal, written, and organizational skills
- Ability to multitask and work independently in a fast-paced environment
- Strong attention to detail and documentation accuracy
- Effective interpersonal and communication skills
- Problem-solving and strategic decision-making abilities
- Leadership skills with a professional and accountable work ethic
Benefits of the Clinical Research Jobs:
- Medical, dental, and vision insurance
- Paid time off and company holidays
- 401(k) retirement plan with company match
- Annual incentive program
- Career development and advancement opportunities
- Supportive, patient-focused clinical research environment
