Clinical Research Coordinator I: Drive Patient-Centric Trials

Velocity Clinical Research, Inc.; Northern (KY); Hybrid; USD 42,000 - 64,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Paid time off

Company holidays

401(k) with company-match

Annual incentive program

Job summary

Velocity Clinical Research is seeking a Clinical Research Coordinator I to conduct and manage clinical trials per protocol, GCP, and Velocity SOPs. You will coordinate startup activities, recruitment, regulatory documentation, and data handling while ensuring patient safety and confidentiality.

The role requires strong organizational and communication skills, ability to multi-task in a fast-paced environment, and the ability to work with sponsors, CROs, and vendors. Local travel may be required.

Qualifications

• Bachelor’s degree with 1 year of relevant experience in the life science industry or equivalent.
• Associate’s degree with 2 years of relevant experience in the life science industry.
• High School Graduate or technical degree with minimum of 3 years relevant experience in the life science industry.

Responsibilities

• Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs.
• Coordinate with supervision for start up, vendor management, recruitment, data entry, and queries resolution.
• Implement research and administrative strategies to manage protocols.
• Communicate professionally with coworkers, leadership, sponsors, CROs, and vendors.
• Maintain confidentiality of patient information and Velocity confidential information.
• Ensure patient safety and proper reporting of adverse events per protocol and SOPs.
• Enter all data into sponsor data portal and resolve queries timely.
• Ensure staff are trained and documented.
• Prepare and submit regulatory documents to Sponsors and IRBs as required.
• Evaluate potential subjects for participation and perform prescreening.
• Execute recruitment strategies defined by Clinical Research Team.
• Understand timelines, endpoints, vendors, and patient populations per protocol.
• Perform clinical duties (drug prep, phlebotomy, etc.) within scope.
• Promote diversity and cultural respect.

Skills

Medical terminology

Microsoft Office

Communication skills

Team player

Detail oriented

Multi-tasking

English proficiency

Problem solving

Adaptability

Education

Bachelor’s degree with 1 year of life science experience

Associate’s degree with 2 years of life science experience

High School or technical degree with 3+ years life science experience

Tools

Microsoft Office

Job description

Velocity Clinical Research is seeking a Clinical Research Coordinator I to conduct and manage clinical trials per protocol, GCP, and Velocity SOPs. You will coordinate startup activities, recruitment, regulatory documentation, and data handling while ensuring patient safety and confidentiality.

The role requires strong organizational and communication skills, ability to multi-task in a fast-paced environment, and the ability to work with sponsors, CROs, and vendors. Local travel may be required.