About this role
The Clinical Trial Associate supports the study start-up and lifecycle by managing document collection, TMF maintenance, and regulatory submissions. They ensure compliance with GCP/ICH and Novartis processes while coordinating with vendors and internal stakeholders.
Requires a degree in a scientific or medical field with preferably at least one year of exposure to clinical operations. Candidates must have basic knowledge of drug development, study start-up workflows, and ICH/GCP requirements.
What they're looking for
Clinical ResearchClinical TrialsLifesciencesPartner Relationship Management (PRM)Project PlanningWaterfall Model
Frequently asked questions
What does a Clinical Trial Associate at Novartis do?
The Clinical Trial Associate supports the study start-up and lifecycle by managing document collection, TMF maintenance, and regulatory submissions. They ensure compliance with GCP/ICH and Novartis processes while coordinating with vendors and internal stakeholders. Requires a degree in a scientific…
What skills does this Clinical Trial Associate role need?
Key skills for this role include Clinical Research, Clinical Trials, Lifesciences, Partner Relationship Management (PRM), Project Planning, Waterfall Model.
How much does a Clinical Trial Associate at Novartis pay?
The employer did not list a salary for this role. Most similar Singapore roles publish their band on the job page.
Is this Clinical Trial Associate role remote, hybrid, or on-site?
This role is on-site, based in Singapore.
How do I apply for this Clinical Trial Associate role?
You can apply directly on Novartis's careers page. ApplyLah can tailor your résumé and cover letter to this exact role in seconds first.