Fast-Paced Clinical Research Coordinator I

Velocity-Clinical-Research,-Inc.; Washington (District of Columbia); On-site; USD 55,000 - 75,000; 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 trials in line with study protocols, GCP, and Velocity SOPs. You will coordinate startups, recruitment, and regulatory documentation while ensuring data integrity and patient safety.

The role requires a bachelor’s or equivalent with relevant life science experience, strong communication, and the ability to multitask in a fast-paced environment.

Qualifications

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

Responsibilities

• Conduct and manage clinical trials per protocol and GCP.
• Coordinate startup, vendor management, subject recruitment, and scheduling.
• Collect regulatory documents and ensure data entry and queries resolution.
• Communicate with sponsors, CROs, and vendors.
• Ensure data is entered into sponsor portals and adhere to SOPs.

Skills

Medical terminology

MS Office

Verbal and written communication

Teamwork

English proficiency

Multi-tasking

Attention to detail

Problem solving

Education

Bachelor’s degree +1 year life sciences experience

Associate’s degree +2 years life sciences experience

High school/technical degree +3 years life sciences experience

Tools

Computers

Fax

Copier

Multi-line telephone

Job description

Velocity Clinical Research is seeking a Clinical Research Coordinator I to conduct and manage trials in line with study protocols, GCP, and Velocity SOPs. You will coordinate startups, recruitment, and regulatory documentation while ensuring data integrity and patient safety.

The role requires a bachelor’s or equivalent with relevant life science experience, strong communication, and the ability to multitask in a fast-paced environment.