Clinical Research Compliance Associate

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

Clinical Research Compliance Associate

Application Deadline: 24 October 2026

Department: Operations

Employment Type: Permanent

Location: Richmond Pharmacology HQ

Description

Job Title: Clinical Research Compliance Associate (CRCA)

Location: London Bridge, SE1

Term: Permanent, Full-time

Salary: Competitive + Benefits (Private Medical, Private Dental, Life Assurance, Private Pension & many more)

Purpose of the job
The CRCA role primarily oversees clinical procedures and ensures accurate, complete data collection adhering to ICH GCP Guidelines, study protocols (CSPs), SOMs, SOPs, and other relevant regulations. CRCA role focuses on promoting, implementing and embedding the culture of ‘Do It Right the First Time’ for the purpose of ensuring clinical research trials and data quality integrity is upheld at the highest standard in accordance with ICH GCP and other regulatory requirements standards. The CRCA role encompasses the transformational aspects of being proactive in adherence of clinical compliance standards in all relevant aspects to clinical study.

The CRCA roles will include the management of all aspects of external monitoring visits, understand the nature of their queries and where applicable verify the validity of such queries in accordance with the ICH GCP standard requirements.

Main duties and responsibilities

External Monitors and Clinical Research Auditors Management and Reporting:

• Support CRCMs in the delivery of induction and refresher training to EMs/CRAs to ensure Richmond processes and systems are well understood


• Coordinate and supporting CRCMs to liaise and coordinate with internal stakeholders with all aspects to EMs/CRAs site visits, ensuring the necessary documentation and information availability; and any query related activities are addressed in a timely manner.

Training and Education:

• Support and coordinate to ensure clinical research team members are up to date to the latest compliance matters and standards


• Be a point of contact for coordination and liaison for CRC team for training needs analysis and organisation of relevant training

Quality Control and Study compliance:

• Maintain a comprehensive planned quality control activities for clinical research activities.


• Perform internal data quality control to ensure:


• the quality of clinical procedures performed, and any study data collected to ensure it is complete, correct and conforms to all requirements, ICH GCP Guidelines


• accuracy of data collection for all study as per Richmond guidelines agreed by PIs and Sponsor where applicable.


• Where applicable and necessary, support in resolution of VDB/EDC queries


• Support CRC team in adoption of Risk Base Quality Management (RBQM) approach through the establishment of robust statistical process control using six sigma methodologies


• Liaising with the Medical Administration Team to ensure Research Physician query resolutions are completed in a timely and satisfactory manner.

Collaboration and Communication:

• Support CRCMs as a liaison between the research team and external monitors, facilitating communication and addressing inquiries or concerns.

Risk Management and Mitigation:

• Manage and maintain risks associated dataset with clinical research activities primarily in compliance perspective

Continuous Improvement and Monitoring:

• Collate and evaluate the effectiveness of the compliance program supporting CRC team performance


• Collectively work with CRCMs to Implement process improvements and best practices

Documentation and Reporting:

• Maintain documentation of compliance activities, audits, and corrective actions.


• Support preparation of compliance reports to the study team, and other stakeholders


• Support in maintaining the tracking of protocol deviations list and undertake trend analysis


• Escalate to Quality Assurance (QA) team for any non-compliance issue and support the investigation, resolution and corrective actions if applicable.

Qualifications and Experience

• BSc or above in Life Sciences, Nursing or Pharmacy (not necessarily registered in the UK)


• Good knowledge of ICH GCP guidelines


• Good knowledge of MHRA early phase accreditations


• Previous data monitoring experience in CRO or pharma for clinical trials (Desired)