About the Role
Richmond Pharmacology is looking for a Clinical Trials Associate (Japanese Speaking) to join our Clinical Operations team in London. This role is essential for supporting our clinical trials involving Japanese-speaking participants, ensuring high standards of data integrity and volunteer safety.

Key Responsibilities

• Act as a primary point of contact and translator for Japanese-speaking volunteers during clinical trials.
• Assist in the preparation and maintenance of the Trial Master File (TMF) and other study-specific documentation.
• Support the clinical team with volunteer recruitment, screening, and informed consent processes.
• Ensure all trial activities are conducted in accordance with ICH-GCP guidelines and UK regulatory requirements.
• Coordinate study schedules and logistics to ensure efficient trial execution.
• Translate clinical documents, including consent forms and participant information sheets, from English to Japanese and vice versa.

Requirements

• Fluency in both Japanese and English (written and spoken) is mandatory.
• Previous experience in clinical research or a healthcare environment is preferred.
• Strong understanding of ICH-GCP guidelines.
• Excellent organisational skills and attention to detail.
• Ability to work effectively within a multi-disciplinary team in a fast-paced environment.

Benefits

• Competitive salary and benefits package.
• Opportunity to work at a world-leading Clinical Research Organisation.
• Professional development and training in clinical trial methodology.

Richmond Pharmacology is an equal opportunities employer. All applicants must have the right to work in the UK.