Remote-Ready Clinical Compliance Specialist

Veeva; Greater London; On-site; GBP 65,000 - 90,000; Full time

Job summary

Veeva Systems is a mission-driven organization transforming the life sciences industry through compliant GCP practices. The Clinical Compliance Operations Specialist will drive and manage audits, ensure adherence to GCP, HIPAA, and CSV, and work with global teams to maintain quality across product lines.

The role includes documenting findings, facilitating remediation, and conducting supplier assessments while supporting continuous improvement in a fast-paced environment.

Qualifications

• Bachelor’s degree or equivalent relevant experience.
• 3+ years in a Clinical QA role in Life Sciences.
• Experience with Quality Management Systems (e.g., documentation and record management, computer system validation, investigations, CAPA programs).
• Working knowledge of Quality Principles as manifested in ISO 9001 or GCP regulations/guidelines.
• Proven technical writing skills.
• Experience using Veeva Development Cloud (Clinical Data) Applications.

Responsibilities

• Verify compliance to applicable policies, procedures, work instructions and regulations in GCP project implementations.
• Perform GxP/Quality review of project records and deliverables.
• Document audit findings and support remediation of audit observations.
• Promote GCP compliance by authoring records (e.g., project audit reports).
• Perform process improvement activities and incident/CAPA investigations.
• Provide quality oversight on regulated activities and deliverables across products and systems.
• Perform supplier assessments to ensure supplier capabilities for regulated products/services.
• Execute other projects/duties to ensure compliance across Veeva’s product line.

Skills

Technical writing

Communication skills

Time management

Decision making

Education

Bachelor’s degree or equivalent relevant experience

Quality Auditor Certification (ASQ CQA or ISO 13485)

Job description

Veeva Systems is a mission-driven organization transforming the life sciences industry through compliant GCP practices. The Clinical Compliance Operations Specialist will drive and manage audits, ensure adherence to GCP, HIPAA, and CSV, and work with global teams to maintain quality across product lines.

The role includes documenting findings, facilitating remediation, and conducting supplier assessments while supporting continuous improvement in a fast-paced environment.