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# Director, Clinical Data Management

- **Company:** Definium Therapeutics
- **Location:** Durham, NC, United States (Remote available)
- **Experience:** Experienced
- **Salary:** $207,709.0 - $235,935.0
- **Contract:** Permanent contract
- **Skills:** Biometrics, Clinical Data Management, Databases, Data Visualization, Database Development, Data Management, GXP
- **Published:** July 12, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=305a5766e4adc6b5

## About the Role

* Ability to meet deadlines, prioritize workload, and handle multiple priorities simultaneously
 * Experience with data visualization tools (e.g., Elluminate) (preferred)
 * Must maintain an inspection-ready environment and support regulatory readiness
 * Willingness to travel as needed, * Bachelor's or Master's degree in a scientific subject area
 * Minimum of 8 years CDM experience in a pharmaceutical, biotech or CRO setting
*

 + At least 4 years of line management experience
 + Global or international experience is required
 * Strong experience in cross functional leadership, clinical trial execution, vendor oversight, and inspection readiness
 * Sophisticated knowledge of CDM processes, EDC systems, database programming, quality management and technology trends
 * In-depth knowledge of FDA regulations, GCP, GCDMP, CDASH/CDISC, and ICH guidelines
 * Strong leadership, mentoring, recruiting and team development skills
 * Excellent communication, interpersonal, influencing and negotiation skills
 * Strong problem-solving, analytical thinking, prioritization and organizational skills
 * Ability to manage multiple priorities, adapt to changing business needs, and work collaboratively across functions

The starting base pay range for this position is $207,709.00 - $235,935.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee's geographic location.

## Description

* Oversee CDM operations including CRF/eCRF design, validation programming, discrepancy management, and database development/production
 * Provide oversight of CROs, vendors, and internal teams to maintain quality standards and performance metrics
 * Ensure CDM documentation, SOPs, and processes support high data quality, integrity, and regulatory compliance with FDA, GCP, ICH, and GCDMP requirements
 * Partner within Biometrics and Data Science as well as cross-functionally on data management issues and alignment
 * Recruit, develop, motivate, and provide leadership to CDM staff and consultants
 * Support resource planning, budget forecasting, timelines, and issue resolution for ongoing clinical trials
 * Identify risks and challenges in clinical trial data management and propose solutions to maintain timelines and quality
 * Escalate strategic, budgetary, or cross-functional issues when broader leadership input is required


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