Clinical Trial Associate

Summary#LI-Hybrid

Location: Singapore

About 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 Description

Key Responsibilities:-

Supports document collection, preparation, and adaption for submission to IRB/EC and Health Authorities as applicable

Sets-up systems, supports vendor selection, documentation processes and data entry

Set-up and maintenance according to regulatory and Novartis requirements, document oversight and tracking, support vendor set-up as applicable

Checks site “Green Light” completeness and ensures all documentation is in place for initial

and 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 material

Responsible 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 operations

At 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 standards

Strong process and system understanding. Self-motivated, structured and committed way of working

Ability to prioritize and high coordination skills. Demonstrated collaboration and communication skills

Commitment to Diversity and Inclusion / EEO paragraph:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams

representative of the patients and communities we serve.

Skills DesiredClinical Research, Clinical Trials, Lifesciences, Partner Relationship Management, Project Planning, Waterfall Model

REQ-10065287