
1001 - 5000 employees
Founded 1999
🧬 Biotechnology
💊 Pharmaceuticals
Biotechnology • Pharmaceuticals
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.
🔥 2 minutes ago
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1001 - 5000 employees
Founded 1999
🧬 Biotechnology
💊 Pharmaceuticals
Biotechnology • Pharmaceuticals
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.
• Independently sources and analyzes data to develop site, country and investigator strategy or recommendations for proposals and post-award feasibility offerings • Advise project teams on all Feasibility activities and/or strategy for clinical studies • Research and apply critical thinking and analysis on the information available for therapeutic area(s) • Conduct timely site follow-up on all aspects of the feasibility process • Prepare presentations independently and/or written reports, as required
• Bachelor’s Degree in allied health field such as nursing, pharmacy or health science or the equivalent relevant experience • At least 5 years relevant pharmaceutical or CRO Clinical Research experience • Global experience • Equivalent combination of education, training and experience
• generous health benefits and vacation packages • hybrid work from home opportunities • paid parental leave • structured mentoring program and leadership courses • ongoing education and training through tuition reimbursement
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