Company · 212 open roles
Careers at CTI
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212 positions at CTI
Senior Biostatistician (up to $10K in sign on bonus!)
CTI·Covington, KY
What You'll Do: • Assist with the development and modification of department SOPs and work instructions • Assist with training new Biostatistics employees; mentor and assist junior level biostatisticians • Develop study bids and changes in scope for Biostatistics tasks in re…
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…
eTMF Spec I
CTI·Lisboa, PRT
What You'll Do: • Oversee and guide eTMF processes and specific timelines assessments for each trial; monitor against trial progress and ensure trial activity is in compliance with relevant processes; suggest and implement alternative solutions for issues identified and take cor…
Research Pharmacist - part time
CTI·Plymouth, MI
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…
Project Manager II/Senior, Real World Evidence/ Late Phase Research
CTI·Covington, KY
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…
Medical Director - Oncology
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…
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…
Agent Magasinier F/H - CTI
CTI·44 - Montoir-de-Bretagne
Vous aimez le travail bien organisé, les environnements techniques et le sentiment de contribuer à des projets d'envergure ? Rejoignez CTI - Calorifuge Thermique Isolation, spécialiste de l'isolation de panoplies et de gaines pour le secteur naval à Saint-Nazaire, et devenez un a…
Specimen Kit Associate
CTI·Cincinnati, OH
What You'll Do • Maintain a working knowledge of different types of collection tubes and kits, e.g., blood collection tubes, aliquots • Maintain kitting department and create an organized workflow to ensure accurate kit building • Assemble kits and all required documentatio…
Clinical Research Associate II
CTI·New Cairo City, EGY
About the job This position is 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 C…
Sr eTMF Analyst (Trial Master File Management)
CTI·New Cairo City, EGY
About the job: Responsible for assisting with the analysis and management of essential trial documentation for multiple regulated projects; Successfully and efficiently analyze and quality control (QC) individual trial/project specific essential regulatory documents What You'll…
eTMF Analyst I (Trial Master File Management)
CTI·New Cairo City, EGY
About the job: Responsible for assisting with the analysis and management of essential trial documentation for multiple regulated projects and developing skills to successfully and efficiently analyze and quality control (QC) individual trial/project specific essential regulator…
Regulatory Affairs Study Start Up Specialist (level dependent on experience)
CTI·Covington, KY
Job Purpose/ Summary: 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. …
Manager, Regulatory Affairs Study Start Up (level dependent on experience)
CTI·Covington, KY
Job Summary: The Regulatory Affairs Study Start-Up Manager provides line management, coaching, and professional development for Regulatory Specialists and Regulatory Coordinators while overseeing the delivery and quality of regulatory and study start-up activities across multiple…
Sample Management Technician
CTI·Bizkaia, ESP
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…
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 …
Sr Statistical Programmer
CTI·New Cairo City, EGY
What You'll Do: • Assist with the development and modification of department SOPs and work instructions • Assist with training new statistical programmer employees; mentor and assist junior level programmers • Assist with the development of study bids and changes in scope fo…
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…
Senior Clinical Research Associate (level dependent on experience)
CTI·Covington, KY
What you'll do: • Serve as the 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 the Monitoring …
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…
Country SSU Spec (Level Depending on experience)
CTI·Ulm, DEU
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/prepare local submission documents and performs submiss…
Sr. Director, Regulatory Affairs Study Start Up (level dependent on experience)
CTI·Covington, KY
This position will be office based at either our headquarters located in Covington, KY or our office in Raleigh, NC. Job Summary: Provides strategic and operational leadership for the global Regulatory Affairs Study Start-Up (RASSU) function, with accountability for organizatio…
Biostatistician II (Clinical Trial Experience Required)
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…
Research Associate
CTI·Covington, KY
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 in…
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