Clinical Research Coordinator I — Fast-Paced Trials

Velocity Clinical Research, Inc.; Greater London; In loco; GBP 26.000 - 34.000; Tempo pieno

Descrizione del lavoro

Velocity Clinical Research seeks a Clinical Research Coordinator I to conduct and manage trials in accordance with protocol, GCP, and Velocity SOPs. You will coordinate start-up, vendor management, recruitment, data entry, and regulatory submissions.

The role requires strong communication, attention to detail, and the ability to work in a fast-paced clinical environment, ensuring patient safety and data quality at all times.

Competenze

• Bachelor’s degree with 1 year of life science experience.
• Associate’s degree with 2 years of life science experience.
• High school diploma with at least 3 years in life sciences.

Mansioni

• Conduct and manage clinical trials per protocol and SOPs.
• Coordinate start-up, vendor management, recruitment, and visits.
• Ensure timely data entry and resolution of queries.
• Report adverse events and deviations per regulatory requirements.
• Prepare regulatory documents and close-out reports.
• Maintain confidentiality of patient and sponsor information.
• Communicate with sponsors, CROs, vendors, and staff.
• Train staff and ensure compliance with GCP/ICH.

Conoscenze

Medical terminology

Team player

Communication

English proficiency

Multi-tasking

Attention to detail

Formazione

Bachelor’s degree, life sciences

Associate’s degree, life sciences

High school diploma/technical degree

Strumenti

Microsoft Office

Descrizione del lavoro

Velocity Clinical Research seeks a Clinical Research Coordinator I to conduct and manage trials in accordance with protocol, GCP, and Velocity SOPs. You will coordinate start-up, vendor management, recruitment, data entry, and regulatory submissions.

The role requires strong communication, attention to detail, and the ability to work in a fast-paced clinical environment, ensuring patient safety and data quality at all times.