Assist with investigations, root cause analyses, corrective actions, and continuous improvement initiatives.
Ensure quality documentation remains accurate, current, and compliant.
Participate in risk assessments and process improvement projects.
Partner with operational teams to promote a strong quality culture across the organisation.
Training & Development
Coordinate and maintain organisation-wide training and competency programs.
Manage training records and compliance tracking.
Support onboarding and induction activities.
Coordinate GCP, SOP, systems, and process-related training.
Ensure all training documentation remains audit-ready and inspection-ready.
Support the development of learning resources and training materials.
Stakeholder Engagement
Act as a trusted point of contact for quality and compliance queries.
Work closely with cross-functional clinical research teams.
Support client-facing quality activities as required.
Build strong relationships across operational and leadership teams.
About You
You will likely bring
Experience working within a CRO, clinical research, or clinical trials environment.
Strong understanding of ICH-GCP requirements.
Hands-on experience supporting clinical quality and compliance activities.
Exposure to Quality Management Systems (QMS).
Experience managing SOPs, CAPAs, deviations, document control, or audit activities.
Excellent organisation and attention to detail.
Strong communication and stakeholder management skills.
A proactive approach and the ability to work independently.
Why Consider This Opportunity?
Join a growing and highly regarded clinical research organisation.
Broad exposure across quality, compliance, training, and operations.
Work directly with experienced industry leaders.
Genuine opportunity to influence processes and contribute to organisational growth.
Strong career development potential as the business continues to expand.
Collaborative culture where individuals are encouraged to take ownership and make a visible impact.
