Clinical Research Coordinator I - Launch Your Trials Career

Velocity-Clinical-Research,-Inc.; Anderson (SC); On-site; USD 42,000 - 60,000; Full time

Benefits offered by this job

Medical, dental and vision insurance

Paid time off

401(k) retirement plan with company‑m‑

Job summary

Velocity Clinical Research in Anderson, SC is seeking a Clinical Research Coordinator I to conduct and manage trials in accordance with the study protocol, GCP, and Velocity’s SOPs. You will coordinate start‑up, subject recruitment, data collection, and regulatory documents while ensuring data integrity and patient safety.

Requirements include a life sciences background and strong organizational skills. The role offers growth in clinical research within a collaborative team, with competitive

Qualifications

• Bachelor's degree with 1 year of relevant experience in life sciences.
• Associate's degree with 2 years of relevant experience in life sciences.
• High School/technical degree with minimum 3 years of relevant experience in life sciences.

Responsibilities

• Conduct and manage clinical trials per protocol, GCP, and SOPs.
• Coordinate start up, vendor management, subject recruitment, visits, and data entry.
• Review regulatory documents and report adverse events and deviations.
• Maintain confidentiality of patient and sponsor information.
• Ensure timely data entry and query resolution in sponsor data portals.
• Prepare regulatory submissions to sponsors and IRBs as required.

Skills

Medical terminology

Microsoft Office

Team player

Attention to detail

English proficiency

Multitasking

Communication skills

Problem solving

Education

Bachelor's degree (life sciences)

Associate's degree (life sciences)

High school/technical degree

Tools

Computers

Microsoft Office

Fax

Copier

Multi-line telephone

Job description

Velocity Clinical Research in Anderson, SC is seeking a Clinical Research Coordinator I to conduct and manage trials in accordance with the study protocol, GCP, and Velocity’s SOPs. You will coordinate start‑up, subject recruitment, data collection, and regulatory documents while ensuring data integrity and patient safety.

Requirements include a life sciences background and strong organizational skills. The role offers growth in clinical research within a collaborative team, with competitive