Clinical Research Compliance Specialist - GCP & Audits

Richmond Pharmacology; Greater London; On-site; GBP 42,000 - 64,000; Full time

Benefits offered by this job

Private Medical

Private Dental

Life Assurance

Private Pension

Job summary

Richmond Pharmacology in London Bridge, SE1 seeks a Clinical Research Compliance Associate to oversee clinical procedures and ensure complete, accurate data collection in line with ICH GCP guidelines, study CSPs, SOMs and SOPs. This permanent, full-time role promotes a culture of doing it right the first time to uphold trial quality and regulatory compliance.

The CRCA will manage external monitoring visits, coordinate training, and support risk-based quality management across studies, working

Qualifications

• BSc or higher in life sciences, nursing or pharmacy.
• Strong knowledge of ICH GCP guidelines.
• Understanding of MHRA early phase accreditations.
• Experience in CRO/pharma data monitoring is desirable.

Responsibilities

• Oversee external monitors and clinical trial audits and reporting.
• Coordinate training to ensure staff understand Richmond processes.
• Maintain quality control activities and ensure data integrity per ICH GCP.

Skills

ICH GCP knowledge

GCP guidelines knowledge

RBQM awareness

Education

BSc or above in Life Sciences, Nursing or Pharmacy

Job description

Richmond Pharmacology in London Bridge, SE1 seeks a Clinical Research Compliance Associate to oversee clinical procedures and ensure complete, accurate data collection in line with ICH GCP guidelines, study CSPs, SOMs and SOPs. This permanent, full-time role promotes a culture of doing it right the first time to uphold trial quality and regulatory compliance.

The CRCA will manage external monitoring visits, coordinate training, and support risk-based quality management across studies, working