Quality Assurance - Clinical Research

Day-to-day responsibilities include reviewing clinical and operational documentation, supporting the development and maintenance of SOPs, performing risk-based quality checks, and monitoring adherence to quality plans across projects. The individual will participate in internal and external audits, assist in investigation and resolution of quality issues, and contribute to continuous improvement initiatives in clinical supply chain operations. Collaboration with cross-functional teams such as project management, regulatory, and operations will be essential to support high-quality execution of global clinical studies.
Qualifications
Candidates should possess strong skills in Quality Assurance and Quality Management, including implementation and oversight of quality systems in a clinical research or life sciences environment.
Candidates should possess hands-on experience in Quality Control, with the ability to perform and interpret quality checks on processes, documentation, and clinical supply chain activities.
Candidates should possess knowledge of Good Manufacturing Practice (GMP) and related regulatory standards, ensuring alignment of clinical trial processes with applicable quality and compliance requirements.
Candidates should possess experience in Quality Auditing, including planning, conducting, and documenting internal and external audits, and following up on corrective and preventive actions.
Relevant qualifications such as a bachelor’s degree in life sciences, pharmacy, nursing, or a related field; prior experience in clinical research, clinical operations, or clinical supply chain; and familiarity with ISO and GxP environments.

Work arrangement
Yes