Sashika Naidoo

Associate Director of Clinical Trials

At GMR, Sashika Naidoo ensures adherence to Good Clinical Practice (GCP) standards in the advancement of medical research. Supported by over 14 years of experience in clinical trials and certifications in ISO 9001 Lead Auditing and HREC training, her expertise spans regulatory compliance, ethical oversight, and quality systems, particularly in the field of oncology.

At GMR, Sashika collaborates with investigators, sponsors, regulators, and ethics committees to facilitate clinical research initiatives that prioritise compliance and participant safety. Her commitment to ethical excellence and passion for oncology trials drives valueable contributions to advancing impactful medical research and improving human health.