Clinical Research Coordinator I — Fast-Paced Trials

Socket.dev; Potomac (MD); On-site; USD 60,000 - 75,000; Full time

Job summary

Velocity Clinical Research is seeking a Clinical Research Coordinator I to conduct and manage trials according to protocol and GCP. You will coordinate start-up activities, vendor relations, subject recruitment, visits, and data collection.

Responsibilities include regulatory document submission, adverse event reporting, and ensuring data integrity. Strong communication, organization, and ability to work in a fast-paced environment are essential.

Qualifications

• Bachelor’s degree with 1 year of relevant life science experience or equivalent.
• Associate’s degree with 2 years of relevant life science experience.
• High School diploma/technical degree with 3 years relevant experience.

Responsibilities

• Conduct and manage clinical trials in accordance with the protocol, GCP and SOPs.
• Coordinate trials including start up, vendor management, recruitment and visits.
• Collect regulatory documents, report adverse events, and implement amendments.
• Maintain data integrity and ensure timely data entry and query resolution.
• Communicate with sponsors, CROs, vendors and study staff professionally.
• Ensure patient safety and regulatory compliance, protect confidentiality.

Skills

Medical terminology

Microsoft Office

Multi-line telephone

Communication skills

Team player

English proficiency

Multi-tasking

Documentation

Problem solving

Professionalism

Education

Bachelor’s degree with 1 year of relevant experience

Associate’s degree with 2 years of relevant experience

High School diploma or technical degree with 3 years relevant experience

Tools

Microsoft Office

Job description

Velocity Clinical Research is seeking a Clinical Research Coordinator I to conduct and manage trials according to protocol and GCP. You will coordinate start-up activities, vendor relations, subject recruitment, visits, and data collection.

Responsibilities include regulatory document submission, adverse event reporting, and ensuring data integrity. Strong communication, organization, and ability to work in a fast-paced environment are essential.