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177 positions at CTI
Sr Clinical Data Manager
CTI·Lisboa, PRT
JOB PURPOSE / SUMMARY This person will serve as the primary CTI Clinical Data Management (CDM) contact with sponsors and represent the DM group on CTI project teams. Responsible for study-specific CDM document development and maintenance, project status to the CTI project team, …
Senior Clinical Research Associate (level dependent on experience)
CTI·Covington, KY
Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies, while continuing to develop knowledge of drug development process, International Council for Harmonisation (ICH) / …
Manager, Risk Based Quality Management
CTI·Covington, KY
Job Summary: Supports the execution, operationalization, sustainability, and continuous improvement of CTI's Risk-Based Quality Management framework across the clinical trial portfolio. This role supports the Director, RBQM by coordinating Integrated Quality and Risk Management P…
Sr Clinical Data Associate
CTI·Lisboa, PRT
What You'll Do: • Conduct pre-entry review of clinical data • Review and issue queries for case report form (CRF) data based on automated edit checks, manual review, and sponsor requirements • Assist with set-up of data management study files and the collection, transfer, an…
Medical Laboratory Technologist - Level Dependent Upon Experience
CTI·Cincinnati, OH
What You'll Do • Perform moderate and high complexity testing, as defined by CLIA, while following the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of test results • Stay current on and adhere to all laboratory p…
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…
Associate Director, Clinical Project Management - up to $25K sign-on bonus!
CTI·Covington, KY
Job Summary: The Associate Director provides leadership role in facilitating the management of the multiple Phase I-IV clinical research trials across all geographic and functional areas; Responsible for ensuring that direct reports and assigned clinical operation's team members …
Clinical Research Associate II / Senior Clinical Research (level dependent on experience)
CTI·London, GBR
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 Research Associate II
CTI·City, BEL
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…
Financial Systems Analyst
CTI·Lisboa, PRT
What You'll 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 requi…
Site Contract Specialist
CTI·Remote, ESP
** Please submit your application in English ** What You'll Do: • Initiate site contact and follow-up as necessary to turn study confidentiality agreements (CDA) and study clinical trial agreement (CTA) drafts • Administer contract language to ensure it remains within appro…
Clinical Scientist - Level Dependent Upon Experience
CTI·Sao Paulo, BRA
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 Scientist - Level Dependent Upon Experience
CTI·Lisboa, PRT
What You'll Do: • Perform medical monitoring activities under the oversight of a medical director. Medical monitoring activities include but not limited to review of the protocol and investigator's brochure, review of medical budgets, preparing the medical monitoring plan, train…
Developer, Lab Applications
CTI·Cincinnati, OH
What You'll Do • Work with system owners to develop requirements and transform LIMS into 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, Sm…
Manager, Site Contracts
CTI·Covington, KY
What You'll Do: • Personnel Management • Manage and develop department personnel as assigned, including performance evaluations and employee relations • Administrative responsibilities relative to personnel management including but not limited to timesheets, tracking, and ti…
Research Associate
CTI·Lisboa, PRT
What You'll 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 i…
Country Study Start-Up Specialist I/ II
CTI·Remote, ESP
** 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…
Research Associate
CTI·Lisboa, PRT
What You'll 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 i…
Principal RASSU Specialist (global RASSU lead)
CTI·Remote, PRT
** 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 regula…
Medical Director - HEMOC/Neurology
CTI·Covington, KY
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 p…
Regulatory Affairs, Study Start Up Specialist II
CTI·Sao Paulo, BRA
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…
Site Contract Specialist
CTI·Sao Paulo, BRA
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…
RASSU Specialist II
CTI·New Cairo City, EGY
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 specifi…
Sr. CRA (Clinical Research Associate)
CTI·Riyadh City, SAU
About the job Responsible for project activities associated with monitoring functions of Phase I through Phase IV clinical research studies and Real World Evidence (RWE) studies, while continuing to develop knowledge of drug development process, International Council for Harmoni…