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 development, fro

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 developing capability and tra

About the job Responsible for planning, designing, implementing, and reporting for Real-World Evidence (RWE) and Health Economics & Outcomes Research (HEOR) studies. This includes working closely with pharmaceutical, medical device, and diagnostics clients, among others in the development of project

About the job: Provide comprehensive administrative support to CTI staff, including scheduling meetings, managing communications, coordinating logistics, and assisting with day-to-day operational tasks to ensure smooth team functioning across regions. What You'll Do: Maintain calendars and schedule

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) / Good Clinical Practi

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 Plan activities, faci

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, CDM management, and s

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, and archiving of study documentat

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 policies and procedures. Pr

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

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 deliver their projec

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

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: 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, training project teams on th

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, Smalltalk, Postgres, SQL, Cr

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 time-off requests Manage training

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 developing capability and tra

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 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/prepare local submission documents

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 developing capability and tra