
1001 - 5000 employees
Founded 1999
💼 Consulting
🏥 Healthcare
🧬 Biotechnology
Consulting • Healthcare • Biotechnology
CTI Clinical Trial and Consulting Services is a full-service contract research organization (CRO) that provides clinical trial execution, regulatory strategy, lab and bioanalytical services, real-world evidence generation, and research center management to biotech and pharmaceutical sponsors. With expertise across Phase I–IV studies and complex therapeutic areas (including rare diseases, cell and gene therapy, oncology, neurology, and transplantation), CTI supports study design, site management, patient recruitment, monitoring, safety/pharmacovigilance, biometrics, and quality assurance. Headquartered in Covington, KY, the company emphasizes integrated, patient-centric approaches and global regulatory guidance to accelerate development and bring therapies to patients.
Selected: 🆕 Date Added.
🕒 3 days ago
Associate Director leading Phase I-IV global clinical trials for CTI, a full-service clinical research CRO. Overseeing project delivery, budgets, quality, sponsors, and clinical operations teams.
🕒 3 days ago
Senior Statistical Programmer developing SAS, SDTM, and ADaM deliverables for CTI, a global clinical research CRO. Leading programming activities across clinical studies and supporting life-changing therapies.
🕒 4 days ago
Senior Clinical Research Associate monitoring clinical trial sites for CTI, a global clinical research CRO. Managing site visits, regulatory documents, investigational products, and study deliverables.
🕒 4 days ago
Clinical Research Associate monitoring German clinical trial sites for CTI. Conducting site visits, managing regulatory documents, investigational products, and remote monitoring activities.
🕒 October 7
Clinical Research Associate monitoring Phase I–IV trials and RWE studies for CTI, a global clinical research organization. Managing sites, regulatory documents, investigational products, and monitoring visits.
🕒 October 6
Lead biostatistician designing and analyzing clinical trials at CTI, a global clinical research CRO. Developing statistical plans, datasets, and regulatory submission materials.
🕒 October 2
Clinical Research Associate monitoring UK clinical trial sites for CTI, a clinical research organization advancing treatments. Conducting site visits, remote monitoring, and regulatory oversight.
🕒 October 1
Remote Contract Specialist managing confidentiality and clinical trial agreements for CTI, a global clinical research organization. Coordinating negotiations, execution, tracking, and regulatory contract files.
🕒 October 1
Clinical Research Associate monitoring Italian clinical trial sites for CTI, a clinical research organization. Conducting site visits, managing trial documents, investigational products, enrollment, and remote monitoring.
🕒 September 30
Clinical Research Associate monitoring German clinical trial sites for CTI. Conducting site visits, regulatory oversight, enrollment support, and investigational-product accountability.
🗣️🇩🇪 German Required
🕒 September 30
Regulatory affairs specialist managing submissions and documentation for CTI’s global clinical trials. Supporting sponsors, sites, and study teams throughout clinical development.
🕒 September 24
Business development director selling CTI clinical trial and regulatory consulting services to biotech and pharma clients. Managing strategic accounts, proposals, sales opportunities, and complex deal closure.
🕒 September 21
Clinical Trial Manager overseeing clinical monitoring, CRAs, metrics, and trial documentation for CTI, a global contract research organization. Managing sponsors, sites, risk planning, and study milestones.
🕒 September 18
Associate Director leading site budget operations for CTI, a global clinical research organization. Overseeing clinical trial budgets, CPMs, payment specialists, sponsors, and regulatory compliance.
🕒 September 15
Senior Clinical Data Manager overseeing clinical trial data operations for CTI. Managing CDM teams, data quality, budgets, deliverables, and sponsor communications from startup through archival.
🕒 September 15
Clinical Project Manager leading global clinical trials for CTI, an organization advancing life-changing medicines. Managing teams, vendors, budgets, compliance, and trial deliverables from start-up through analysis.
🕒 September 11
Clinical data management director leading CDM teams, standards, resources, and client delivery. Overseeing clinical trial data operations for a clinical research organization.
🕒 September 2
Clinical Research Associate II monitoring clinical trials for CTI, a global clinical research CRO. Managing sites, regulatory documents, investigational products, monitoring visits, and Lead CRA activities.
🕒 August 28
RASSU Specialist supporting regulatory submissions, compliance, and documentation for clinical-trial study start-up at global CRO CTI. Coordinating sponsors, sites, and regulatory bodies across countries.
🕒 August 18
Senior Biostatistician leading clinical-trial design, programming, and statistical reporting for CTI, a global full-service clinical research CRO. Overseeing SDTM/ADaM analyses, regulatory submissions, and project delivery.
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