Epicareer Might not Working Properly
Learn More

Clinical Trial Associate

Salary undisclosed

Apply on

Availability Status

This job is expected to be in high demand and may close soon. We’ll remove this job ad once it's closed.


Original
Simplified
Job Description Summary Internal Role Title: Clinical Trial AssociateLocation: Singapore #LI-HybridAbout the Role:The Clinical Trial Associate (CTA) supports SSO Study Start-Up Manager and SSO Clinical Project Manager in assigned studies during set-up and whole study lifecycle in compliance with Novartis processes, GCP/ICH and regulatory requirements.Job DescriptionKey Responsibilities:-Supports document collection, preparation, and adaption for submission to IRB/EC and Health Authorities as applicableSets-up systems, supports vendor selection, documentation processes and data entrySet-up and maintenance according to regulatory and Novartis requirements, document oversight and tracking, support vendor set-up as applicableChecks site “Green Light” completeness and ensures all documentation is in place for initialand subsequent drug release in collaboration with the local Qualified Person(s)Supports preparation and translation of ICF into local languages. Supports preparation of patient facing materialResponsible for completeness of uploaded trial related documents.Supports country SSU strategy in close collaboration with SSU Team Lead and SSU Managers to ensure SSU timelines and deliverables are met according to country commitments. Ensures adherence to financial standards, prevailing legislation, health authority and requirements.Provides logistic support to SSU CRA, CRA, CPM, SSU Manager in all phases of the clinical trial. Implements innovative and efficient processes which are in line with Novartis strategy.Essential Requirements:-Commercial or medical training (e.g., vocational qualification, bachelor’s degree), Medical records administrator or equivalent education, preferably with experience in clinical operationsAt least 1 year of relevant working experience.Understanding of the international aspects of drug development process, including strong knowledge of international standards (GCP/ICH), health authorities (FDA/EMA), local/National Health Authorities regulations and Novartis standardsStrong process and system understanding. Self-motivated, structured and committed way of workingAbility to prioritize and high coordination skills. Demonstrated collaboration and communication skillsWhy Novartis?Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here:You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.Commitment to Diversity & Inclusion:We are committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here:Skills Desired Clinical Research, Clinical Trials, Lifesciences, Partner Relationship Management, Project Planning, Waterfall Model