
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.
🕒 March 28
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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.
• Plan, implement, evaluate, and complete full execution of assigned clinical trials; often functions as a global trial lead • Set goals, and timelines, provide oversight and positive leadership to foster motivation within the team • Provide oversight and coordination of the operational aspects of the functional areas on assigned projects to ensure compliance • Provide management of a full scope clinical trial projects including global trials from start-up through analysis phase • Provide coordination of a clinical trial project including organization, implementation, and management of scoped activities • Evaluate and manage project budget against project milestones and scope • Regularly assess project profit margins and work with the trial-assigned Director and project team to understand deficiencies • Prepare or provide oversight and guidance in the development of trial required deliverables • Serve as client contact at project operational level • Provide oversight to contracted vendors and review specifications
• Bachelor’s degree in allied health fields such as nursing, pharmacy, health or natural sciences • At least 6 years of clinical research experience (CRO CRA or Research Manager, Site Research Manager, Central Clinical Research Laboratory Manager) • Graduate degree preferred • Previous technical and managerial experience in conducting clinical pharmaceutical research studies in a hospital setting, a pharmaceutical company, or CRO • Previous CRA experience preferred • Experience or education indicating knowledge of medical and pharmaceutical terminology preferred • Previous experience in a Clinical Project Manager or Clinical Trial Manager level position preferred
• Health benefits • Paid time off • Professional development opportunities • Tuition reimbursement • Flexible work from home opportunities • Paid parental leave
Apply Now🕒 March 27
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