
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.
🔥 16 hours ago
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• Lead management of multiple Phase I-IV clinical research trials across geographic and functional areas • Ensure projects are delivered on time, within budget, and with acceptable quality • Plan, implement, facilitate, and evaluate assigned clinical trials from planning through analysis • Oversee clinical trial operations, deliverables, timelines, budgets, resources, and project teams • Ensure compliance with ICH guidelines, GCP, regulatory guidelines, and trial procedures • Coordinate activities among clinical project managers, clinical project coordinators, functional areas, clients, sponsors, and executive management • Serve as senior project interface with CTI executive management and sponsors • Identify, escalate, and help resolve trial, staff, budget, scope, and operational issues • Review study plans, project timelines, status reports, sponsor deliverables, quality assurance reports, and project metrics • Oversee project team training and provide supervision, guidance, mentoring, and professional development • Support scope changes, contract amendments, budget preparation, new business proposals, client presentations, recruitment, and marketing activities • Lead process improvement initiatives and develop reference and resource materials for clinical operations staff
• Bachelor’s degree in allied health fields such as nursing, pharmacy or health science, preferably with clinical trial management experience, or an equivalent combination of education and relevant work experience • At least 10 years of clinical research experience and/or experience in clinical project management • Clear and thorough understanding of global trial management processes and the operation of all clinical trial functional areas • Experience in management of clinical trials • Thorough and current understanding of at least one therapeutic area for which CTI is contracted for clinical projects preferred
• Structured mentoring program and leadership courses • Tuition reimbursement • Dedicated training department • Generous health benefits • Vacation packages • Hybrid work from home opportunities • Paid parental leave • CTI Cares program • Work-life balance support
Apply Now🕒 Yesterday
Strategic Account Executive growing Medline’s healthcare account sales across Illinois, Minnesota, Iowa, Wisconsin and Missouri. Managing strategic contracts, RFPs, pricing, profitability and customer relationships.
🇺🇸 United States – Remote
💵 $116k - $174k / year
💰 Private Equity Round on 2021-06
⏰ Full Time
🟠 Senior
🔴 Lead
👨⚕️ Medical Director
🕒 5 days ago
51 - 200
Senior Director leading clinical data management for Kailera’s obesity and related-condition therapies. Driving global data integrity, regulatory readiness, CRO oversight, and team growth.
🇺🇸 United States – Remote
💵 $241k - $295k / year
🔥 Funding within the last year
💰 $600M Series B - Kailera Therapeutics on 2025-10
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🕒 5 days ago
Director leading field medical affairs for GondolaBio’s genetic-disease therapeutics. Guiding HCP engagement and MSL execution for Portal’s EPP/XLP program.
🇺🇸 United States – Remote
💵 $249k - $454k / year
💰 $300M Venture Round - GondolaBio on 2024-08
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🕒 5 days ago
Associate Director managing clinical drug supply strategies, packaging, labeling, and shipments for Elevar Therapeutics’ global biotech trials. Ensuring timely, compliant supply across clinical sites.
🇺🇸 United States – Remote
💵 $150k - $185k / year
💰 $20M Venture Round - Elevar Therapeutics on 2018-07
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🕒 6 days ago
Senior Director providing medical oversight for asthma and COPD trials at an AI-driven protein drug design company. Ensuring patient safety, regulatory rigor, and late-stage execution.
🇺🇸 United States – Remote
💵 $277k - $400k / year
💰 $370M Series B on 2021-11
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
🦅 H1B Visa Sponsor