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Expect scenarios on document control, site follow-up, and escalating deviations. Prepare examples of accuracy under deadlines, stakeholder communication, and how you prioritize competing trial tasks.
Strong fit if you are detail-oriented, comfortable with process-heavy work, and ready for on-site Singapore trial support at Novartis ACC without relying on remote flexibility.
As a Clinical Trial Associate at Novartis ACC in Singapore, a typical day centers on trial operations support: tracking study documents and site status, coordinating with clinical teams and vendors, checking protocol and regulatory files for completeness, and logging issues so investigators and monitors can act quickly. Work is on-site in Singapore rather than remote.
Focus on GCP basics, trial documentation (eTMF/ISF concepts), query tracking, and clear written updates. Free options:
No. The listing marks the Clinical Trial Associate role as on-site in Singapore.
Trial documentation, status tracking, and coordination with clinical and vendor partners so studies stay audit-ready.
Saylor Academy Health Sciences courses (free) and Coursera audit-track healthcare courses (free to learn).
Clinical Trial Associate | Novartis ACC | Singapore About This Position The Clinical Trial Associate (CTA) supports SSO Study Start-Up Manager, Study Start-up CRA and Clinical Research Associate in assigned studies during set-up and the whole study lifecycle. Responsibilities include ensuring compliance with Novartis processes, GCP/ICH, and regulatory requirements. Key Responsibilities Support SSO Study Start-Up Manager, Study Start-Up CRA, and Clinical Research Associate in assigned studies. Ensure set-up and execution of clinical trials are compliant with Novartis processes, GCP/ICH, and regulatory requirements. Contribute to the overall success of the study lifecycle from start-up through close-out. Requirements Bachelor's degree in a relevant field such as Life Sciences or related discipline. Minimum 1-3 years of experience in clinical research, preferably with pharmaceutical companies. Familiarity with GCP/ICH guidelines and regulatory requirements for clinical trials. Strong organizational skills and attention to detail. Excellent communication and interpersonal skills. Why Join Novartis ACC At Novartis ACC, you will be part of a dynamic team committed to advancing healthcare. Our culture values innovation, collaboration, and integrity. As a CTA, you will have the opportunity to contribute to groundbreaking research and make a significant impact on patient care. Next Steps To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.
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