Advanced Clinical Research Coordinator — Impactful Trials

Velocity Clinical Research, Inc.; Greater London; On-site; GBP 32,000 - 42,000; Full time

Job summary

Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator II to manage multiple trials from startup to closeout in line with the protocol, GCP, and Velocity SOPs.

You will coordinate site activities, recruit and prescreen subjects, collect regulatory documents, report adverse events, ensure timely data entry, and collaborate with sponsors, CROs, and vendors. Strong organizational, communication, and problem-solving skills are essential.

Qualifications

• Bachelor’s degree with 2 years relevant life science experience or equivalent.
• Associate’s degree with 4 years relevant life science experience.
• High school or technical diploma with 6+ years life science experience and 1 CRC role.

Responsibilities

• Conduct and manage clinical trials in accordance with protocol, GCP, ICH guidelines and Velocity SOPs.
• Coordinate trial start-up, vendor management, subject recruitment, source development review and protocol training.
• Collect regulatory documents, conduct visits, ensure timely data entry and resolve queries.
• Manage and report adverse events and protocol deviations; implement amendments and close-out reports.
• Apply project management concepts to reduce risk and improve quality in trial conduct.
• Communicate professionally with coworkers, sponsors, CROs, and vendors.
• Maintain confidentiality of patient and sponsor information; ensure data is transferred to sponsor data capture systems.

Skills

Medical terminology

MS Office

Fast-paced environment

Verbal communication

Written communication

Team player

English proficiency

Time management

Attention to detail

Problem solving

Education

Bachelor’s degree + 2 years life sciences experience

Associate’s degree + 4 years life sciences experience

High school diploma + 6 years life science + 1 CRC experience

Job description

Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator II to manage multiple trials from startup to closeout in line with the protocol, GCP, and Velocity SOPs.

You will coordinate site activities, recruit and prescreen subjects, collect regulatory documents, report adverse events, ensure timely data entry, and collaborate with sponsors, CROs, and vendors. Strong organizational, communication, and problem-solving skills are essential.