CTI

** Please submit your application in English ** What You'll Do: The Global RASSU Lead will serve as a subject matter expert for clinical trial regulatory requirements, ensuring alignment with country-specific requirements, CTI and sponsor SOPs, ICH/GCP, and applicable regulations. The role will also

Job Purpose The Medical Director will be responsible for growing and leading a therapeutic portfolio through their medical and clinical development expertise and by providing medical and safety monitoring of awarded clinical trials. The Medical Director will be responsible for playing a leadership r

What You'll 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 documents according each coun

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 lifecycle of develo

What you'll do: Develop and lead the global study start-up and site activation strategy for assigned trials, including activation assumptions, country and site sequencing, critical path dependencies, milestone projections, and mitigation plans. Establish, maintain, and communicate country and site a

** Please submit your application and CV in English ** What You'll Do: Plan, implement, evaluate, and complete full execution of assigned clinical trials; often functions as a global trial lead. Set goals, and timelines, provide oversight and positive leadership to foster motivation within the team

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 lifecycle of develo

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 lifecycle of develo

About the job The Clinical Project Manager II (CPM II) is responsible for management and oversight of assigned clinical research trials (Phase I through Phase IV) to ensure client’s goals of time, cost, and quality performance are met. The CPM II is expected to perform most tasks independently but s

What You'll Do: Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applica

Please do not apply if you are not fully eligible to work in Australia. CTI doesn't offer any Sponsorship. What you’ll do: Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country requirements and document any activity discov

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 of development, fro

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 lifecycle of develo

What You'll Do: Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applica

What will you do? Work with system owners to develop and maintain LabWare LIMS as a usable system within the systems development life cycle (SDLC) framework. Develop, test, and maintain LIMS databases, user interfaces, and internal/external reports using LIMS Basic, Smalltalk, Postgres, SQL, Crystal

What You'll 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, feed

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 lifecycle of develo

What You’ll Do: Lead global Medical Affairs and RSA teams with clarity of vision and purpose. Develop and maintain departmental global business plans. Meet or exceed department sales and revenue objectives. Participate in Business Development (BD) capabilities presentations, prepare for and attend c

What you'll do: Obtain vital signs; perform ECGs and other clinical procedures Work closely with Clinical Research Coordinators to complete source documentation, case report forms and other study specific documents completely, accurately and in accordance with site SOPs, Clinical Trial Protocol, and

Under the direction and mentorship of our Clinical Director, Global Laboratory Services, this position is responsible for providing effective clinical leadership for the development and delivery of global laboratory services and products. This position is responsible for clinical oversight of the No