Clinical Research Coordinator I: Fast-Paced Trials & Growth

Velocity Clinical Research, Inc.; United Kingdom; A distancia; GBP 28.000 - 40.000; Jornada completa

Descripción de la vacante

Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator I to conduct and manage clinical trials in line with the study protocol, GCP, and Velocity SOPs. You will coordinate start-up activities, vendor management, recruitment, data entry, and regulatory submissions.

The role emphasizes adherence to data integrity, patient safety, and timely communication with sponsors, CROs, and study teams, with opportunities for professional growth within a supportive team.

Formación

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

Responsabilidades

• Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
• Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.
• Implement research and administrative strategies to successfully manage assigned protocols
• Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors
• Apply good documentation practices when collecting and correcting data, transferring data to sponsor/CRO data capture systems, and resolving queries
• Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
• Ensure patient safety is upheld and all adverse events, serious adverse events, and adverse events of special interest are followed and reported in accordance with the protocol and Velocity SOPs
• Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner
• Ensure staff are delegated and trained appropriately and documented
• Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements
• Evaluate potential subjects for participation in clinical trials including phone and in person prescreens
• Execute recruitment strategies defined by Clinical Research Team
• Understand key timelines, endpoints, required vendors, and patient population for each assigned protocol
• Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope
• Promote respect for cultural diversity and conventions with all individuals

Conocimientos

Medical terminology

Microsoft Office

Organizational skills

Verbal and written communication

Teamwork

Multitasking

Adherence to guidelines

Attention to detail

Problem solving

Flexibility

Educación

Bachelor’s degree + 1 year life science experience

Associate’s degree + 2 years life science experience

High School diploma + 3 years life science experience

Herramientas

Microsoft Office

Descripción del empleo

Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator I to conduct and manage clinical trials in line with the study protocol, GCP, and Velocity SOPs. You will coordinate start-up activities, vendor management, recruitment, data entry, and regulatory submissions.

The role emphasizes adherence to data integrity, patient safety, and timely communication with sponsors, CROs, and study teams, with opportunities for professional growth within a supportive team.