Remote Associate Director, Clinical Data Management

Worldwide Clinical Trials Holdings, Inc.; Wilmington (DE); Remoto; USD 119.000 - 236.000; Tempo pieno

Descrizione del lavoro

Worldwide Clinical Trials is seeking an Associate Director, Clinical Data Management. This leadership role guides Data Management leaders, ensuring high-quality data delivery for clinical trials while driving process improvements and regulatory compliance.

You will oversee budgets, resource planning, and cross-functional collaboration, shaping a high-performing team focused on quality and operational excellence across global studies.

Competenze

• Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or equivalent experience.
• 12+ years of experience in clinical data management or related roles in pharma/biotech/medical devices.
• 6–8 years of line management experience with high-performing teams.
• Expert knowledge of CDM practices, technologies, and regulatory expectations for clinical trials.

Mansioni

• Lead and mentor Data Management leaders to drive performance, engagement, and development.
• Ensure compliance with regulations (GCP), sponsor requirements, and Worldwide SOPs.
• Oversee resource allocation and workforce planning across projects.
• Monitor delivery, identify risks, and implement mitigation strategies to keep programs on track.
• Manage departmental quality, issue management, and continuous improvement initiatives.
• Provide strategic oversight of budgets, profitability, and resource utilization.

Conoscenze

Leadership

Data management

Regulatory knowledge

Budget management

Communication

Problem solving

English proficiency

Formazione

Bachelor's degree or higher in biomedical sciences / life sciences / computer science

Strumenti

Clinical data management systems

Descrizione del lavoro

Worldwide Clinical Trials is seeking an Associate Director, Clinical Data Management. This leadership role guides Data Management leaders, ensuring high-quality data delivery for clinical trials while driving process improvements and regulatory compliance.

You will oversee budgets, resource planning, and cross-functional collaboration, shaping a high-performing team focused on quality and operational excellence across global studies.