Director, Clinical Data Management
CTI Clinical Trial and Consulting Services - Covington, KY
Hiring: Director, Clinical Data Management Company: CTI Clinical Trial and Consulting Services Location: Covington, KY Job Posted Time: 2026-09-12 10:34:23 Employment Type: Contract / Hybrid About the job Experience: •At least 8 years direct line management experience •Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department. •Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market. Required Skills: •Actively facilitate and support development of CDM Global Standard Operating Procedures (GSOPs) •Prepare and defend study specific fee estimates to clients, present CDM capabilities to clients, and communicate project progress, staffing and resource allocation to Senior Director, Data Management •Plan and execute a resource plan that supports the business; identify technology needs or other gaps; identify and communicate risks to the business and develop solution-oriented approaches to address or mitigate risk; trouble-shoot responsibility by resolving critical issues that impact optimal functioning of the team •Provide direction of activities of Clinical Data Management (CDM) team members regarding completion of project deliverables to ensure they are on schedule according to quality standards, requirements, and project budget from study start-up through archival •Provide direct supervision, guidance, and mentoring to CDM staff while encouraging independence and refining skills of staff •Provide effective and timely feedback to management for performance reviews of project team members on an ongoing basis •Maintain open communication with internal and external customers by contacting sponsor counterpart on agreed-upon schedule, responding to correspondence promptly and within agreed upon timeframes, and choosing method of communication based on urgency and type of information including governance calls with Sponsors •Evaluate team requests by considering factors such as efficiency, quality, budget, resources, and customer relations before committing to an action; seek out existing knowledge prior to developing new methods Qualifications: •Knowledge of Data Management systems including Medidata Rave, OmniComm TrialMaster, and IBM Clinical Development •BA/BS in Life Sciences with at least 12 years of experience in CDM or Master’s degree with at least 10 years of experience Compensation: •Flexible work environment (work from home / hybrid options) Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!