Clinical Research Assistant: Drive Innovative Trials

Velocity-Clinical-Research,-Inc.; High Wycombe; On-site; GBP 22,000 - 28,000; Full time

Job summary

Velocity Clinical Research in the UK seeks a Clinical Research Assistant to support the Clinical Operations Team in conducting clinical studies, performing clinical, laboratory, administrative and data management tasks. You will help collect, document and maintain trial data in line with UK GCP, MHRA requirements and SOPs.

You will participate in source data entry, specimen handling under supervision, and help with participant recruitment, regulatory filings and study documentation while

Qualifications

• GCSEs in English and Maths are required.
• Experience in healthcare, clinical research, or life sciences is desirable.
• Desirable Level 3 qualification in life sciences, healthcare or a scientific discipline.
• Knowledge of GCP principles is beneficial.

Responsibilities

• Assist in conducting clinical trials per study protocols and MHRA requirements.
• Perform venepuncture and other specimen collection procedures as trained.
• Support clinical assessments including vital signs and ECGs under supervision.
• Enter source data into sponsor/vendor electronic systems and assist with data queries.
• Maintain documentation in accordance with Good Documentation Practice and SOPs.
• Support participant recruitment, retention and pre-screening activities.
• Maintain confidentiality per UK GDPR and Data Protection Act 2018.

Skills

Medical terminology

Verbal communication

Written communication

Organisational skills

Time-management

Team collaboration

Regulatory compliance

Data entry

Microsoft Office

Education

GCSE English & Maths

Level 3 qualification in life sciences

Tools

Electronic data capture (EDC) systems

Job description

Velocity Clinical Research in the UK seeks a Clinical Research Assistant to support the Clinical Operations Team in conducting clinical studies, performing clinical, laboratory, administrative and data management tasks. You will help collect, document and maintain trial data in line with UK GCP, MHRA requirements and SOPs.

You will participate in source data entry, specimen handling under supervision, and help with participant recruitment, regulatory filings and study documentation while