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212 positions at CTI
Clinical Research Associate (level dependent on experience)
CTI·France, FRA
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 whi…
Clinical Project Coordinator
CTI·Raleigh, NC
Job Summary: The Clinical Project Coordinator position is responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, budgets and quality standards are being achieved. **Please note that this position is office based to be filled …
Clinical Project Manager II
CTI·New Cairo City, EGY
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 th…
Clinical Research Associate - CRA (Level Depending on Experience)
CTI·Sydney, NSW, AUS
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 th…
Clinical Trial Manager
CTI·Covington, KY
What You'll Do • Review scope of project and resourcing related to Clinical Monitoring with Clinical Project Management • Plan, schedule, and implement the clinical monitoring aspects of projects • Define and implement project-specific functional standards, goals, and expectat…
Director, Modeling Informed Drug Development
CTI·Covington, KY
Job Purpose/ Summary: The Director, Model Informed Drug Development/ Consulting is a senior individual contributor responsible for leading modeling and simulation activities within drug development programs. The incumbent applies advanced pharmacometric methodologies to support d…
Research Scientist II PKPD
CTI·Remote, ESP
** Please submit your application and CV in English ** What You'll Do: • Act as principal investigator in the context of GLP studies ensuring compliance • Conduct preclinical and clinical pharmacokinetic (PK) Non-compartmental Analysis (NCA) independently using Phoenix Win…
Senior Accountant
CTI·New Cairo City, EGY
What You'll Do: • • Review and process supplier invoices, ensuring proper approvals and supporting documentation. • Review contracts and validate payment terms before processing payments. • Prepare and process vendor and consultant payments in a timely manner. • Perform ba…
Senior Regulatory Affairs Study Start Up Specialist
CTI·Covington, KY
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 perf…
Regulatory Affairs Study Start Up Specialist II
CTI·Sydney, NSW, AUS
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 requireme…
Clinical Project Manager
CTI·Sydney, NSW, AUS
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…
Clinical Project Coordinator/Clinical Trial Assistant
CTI·Sydney, NSW, AUS
What You'll 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 items, and …
Country Study Start-Up Specialist I
CTI·Milano, ITA
** Please submit your application in English ** What You'll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: • Informs the RASSU department about any change of Drug Law/guidelines and updated requirements for submission on the country level • Review/pre…
Biostatistician II
CTI·Lisboa, PRT
What You'll 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 project budget and time…
RASSU Coordinator
CTI·Lisboa, PRT
What You'll 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 contacting sites to obtain ma…
Project Manager, Laboratory Services
CTI·Bizkaia, ESP
What You'll Do: • Plan, implement, evaluate, and complete execution of assigned laboratory clinical trials/projects; may function as a global lead, where applicable. Expected to manage medium to high complexity trials. • Set goals and timelines, provide oversight and foster mot…
Clinical Research Associate II / Senior Clinical Research (CRA) (m/w/x) Germany
CTI·Ulm, DEU
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 whi…
Sample Management Technician
CTI·Cincinnati, OH
What You'll Do • Perform receipt, handling, storage, retrieval, disposition and tracking of samples • Enter associated sample data into the Laboratory Information Management System (LIMS) and ensure accuracy • Pull required samples for organization and shipping of samples and/…
Developer Lab Applications
CTI·Bizkaia, ESP
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, Smallt…
Biostatistician II
CTI·New Cairo City, EGY
What You'll 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 project budget and ti…
Resource Specialist
CTI·New Cairo City, Cairo Governorate, Egypt
Resource Specialist at CTI. Location: New Cairo City, Cairo Governorate, Egypt. Role: aligning personnel, forecasting resources, managing schedules Requirements: Bachelor's degree or equivalent; familiarity with FinancialForce, FinancialForce Resource Planner, Salesforce, and Exc…
Resource Specialist
CTI·New Cairo City, EGY
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 provid…
Resource Specialist
CTI·Sydney, New South Wales, Australia
Resource Specialist at CTI. Location: Sydney, New South Wales, Australia. Role: aligning personnel, forecasting resources, managing schedules Requirements: Bachelor's degree or equivalent; strong verbal/written communication, organizational skills, and proficiency with FinancialF…
Resource Specialist
CTI·Sydney, NSW, AUS
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…