What Youll Do: Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings Review and adapt study specific
What Youll Do Support Clinical Project Manager / Director in completing management activities; supports activities through all phases of a clinical project; provide back-up management as needed Update Clinical Project Manager / Director on progress, outstanding
What Youll Do Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings Review and adapt study specific
What Youll Do: Assist in organizing, composing, and producing professional letters, summaries, reports, minutes, etc, using Microsoft Office software including Word, Access, and Excel Proofread documents ensuring grammar, spelling, and punctuation are correct Assist in developing
What Youll Do: Provide first-level support to all CTI employees for computer system hardware, software, and telecommunications Procure and install all new electronic devices such as PCs; set up as required Meet with all new employees and
What Youll Do Collaborate with the Manager, Resource Management, department leaders, line managers, and Business Development to align personnel with business needs. Maintain regular communication with Manager, Resource Management and cross-functional leadership to provide departmental updates,
What Youll Do: As the lead Biostatistician on the studies assigned, perform the following tasks: Act as primary statistical contact for internal and external project team members. Communicate and work with Biostatistics management to maintain the
What Youll Do: Assist in compilation and revision of Regulatory Affairs (RA) documents required for clinical trials submissions Assist in the contact with local study teams for RA documents collection and checks, when applicable Assist in
What Youll Do: Support the administration and maintenance of financial systems, including Sage Intacct, Concur, and Certinia (FinancialForce) Assist with maintaining resource records, user access, roles, and permissions in compliance with internal controls and audit requirements.
About CTI 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
Please do not apply if you are not fully eligible to work in Australia. CTI doesnt offer any Sponsorship. What you’ll do: Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to
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 lifecycle
Job Purpose/ Summary: Independently manage essential regulatory documentation (as applicable) for submission to country/regional/site Institutional Review Boards (IRB), Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies for all clinical studies performed globally. Interact with,
A global manufacturing firm is looking for a Customs and Trade Compliance Specialist to manage international trade compliance activities across Canada, the U.S., Mexico, and China. The role demands strong skills in tariff classification and customs