Clinical Trial Associate

6 days ago

Singapur, Singapore Novartis Singapore Full time

About The Role The Clinical Trial Associate (CTA) supports the SSO Study Start‑Up Manager and SSO Clinical Project Manager in assigned studies during set‑up and the entire study lifecycle in compliance with Novartis processes, GCP/ICH and regulatory requirements. Location: Singapore Key Responsibilities Supports document collection, preparation and adaptation for submission to IRB/EC and Health Authorities as applicable. Sets up systems, supports vendor selection, documentation processes and data entry. Maintains regulatory and Novartis requirements, document oversight and tracking; supports 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 and prepares patient‑facing material. Ensures completeness of uploaded trial‑related documents and supports the country SSU strategy in collaboration with the SSU Team Lead and SSU Managers to meet SSU timelines and deliverables. Provides logistic support to SSU CRA, CRA, CPM and SSU Manager in all phases of the clinical trial, implementing innovative and efficient processes aligned 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 drug development process, including strong knowledge of GCP/ICH, health authorities (FDA/EMA), local/National Health Authority regulations and Novartis standards. Strong process and system understanding; self‑motivated, structured and committed way of working. Ability to prioritize and coordinate at a high level; demonstrated collaboration and communication skills. Commitment to Diversity and Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Benefits and Rewards Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: Apply To apply, visit Novartis Careers or sign up for our talent community to stay connected and learn about suitable career opportunities as they arise: #J-18808-Ljbffr

  • Clinical Project Manager

    1 week ago

    Singapur, Singapore CTI Clinical Trial and Consulting Services Full time

    Overview Clinical Project Manager role at CTI Clinical Trial and Consulting Services. CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the...

  • Clinical Trial Manager

    1 week ago

    Singapur, Singapore Medpace Full time

    Join to apply for the Clinical Trial Manager (Oncology) role at Medpace Continue with Google Continue with Google Join to apply for the Clinical Trial Manager (Oncology) role at Medpace Medpace is currently looking for Clinical Trial Manager (CTM) to lead global clinical research studies. This position is fully office-based in our Singapore office. Medpace...

  • Clinical Trial Associate

    6 days ago

    Singapur, Singapore Novartis Full time

    Summary #LI-Hybrid Location: Singapore The Clinical Trial Associate (CTA) supports SSO Study Start‑Up Manager and SSO Clinical Project Manager in assigned studies during set‑up and the whole study lifecycle in compliance with Novartis processes, GCP/ICH and regulatory requirements. About the Role Key Responsibilities Supports document collection,...

  • Associate Clinical Trial Manager

    1 week ago

    Singapur, Singapore Medpace Full time

    Associate Clinical Trial Manager - PhD / Post-Doc (Oncology) Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our Singapore office. The aCTM will be a part of the...

  • Associate Clinical Trial Manager

    1 week ago

    Singapur, Singapore Medpace Full time

    Associate Clinical Trial Manager - PhD / Post-Doc - Infectious Disease Join to apply for the Associate Clinical Trial Manager - PhD / Post-Doc - Infectious Disease role at Medpace Associate Clinical Trial Manager - PhD / Post-Doc - Infectious Disease 1 week ago Be among the first 25 applicants Join to apply for the Associate Clinical Trial Manager - PhD /...

  • Associate Clinical Trial Manager

    1 week ago

    Singapur, Singapore Medpace Full time

    Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology) Join to apply for the Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology) role at Medpace Associate Clinical Trial Manager (PhD, nuclear medicine / radiopharmaceuticals / radiation oncology) Join to apply for...

  • Associate Clinical Trial Manager

    2 weeks ago

    Singapur, Singapore Medpace Full time

    Job Summary Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our Singapore office. The aCTM will be a part of the Clinical Trial Management team and support Project...

  • Associate Clinical Trial Manager

    2 weeks ago

    Singapur, Singapore Medpace Full time

    Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience in nuclear medicine/radiopharmaceuticals/radiation oncology for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in Singapore. The aCTM will be a part of the Clinical Trial Management team working with Project...

  • Clinical Trial Manager FSP

    6 days ago

    Singapur, Singapore Parexel International Full time

    Key Accountabilities Trial Preparation Accountable for the trial activities for responsible R/OPU, including but not limited to; Verify the trial is conducted in compliance with GCP-ICH, local/global regulations, application SOPs and according to the trial protocol by overseeing CRO and internal team activities. Creation, management and review of the R/OPU...

  • Clinical Trial Manager FSP

    4 days ago

    Singapur, Singapore Parexel Full time

    1 day ago Be among the first 25 applicants Key Accountabilities Accountable for the trial activities for responsible R/OPU, including but not limited to; Verify the trial is conducted in compliance with GCP-ICH, local/global regulations, application SOPs and according to the trial protocol by overseeing CRO and internal team activities. Creation, management...