Remote Associate Director, Clinical Data Management

Worldwide Clinical Trials

Wilmington (NC)

Remote

USD 119,000 - 236,000

Full time

5 hours ago
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Job summary

Worldwide Clinical Trials, a global CRO, seeks an Associate Director of Clinical Data Management to lead data management strategy, operations, and quality across trials. You will drive compliance, resource planning, and timely delivery while shaping departmental processes and talent development.

You will collaborate with stakeholders across multiple time zones in a remote US-based role, ensuring high-quality data for clinical research and patient outcomes.

Qualifications

  • Bachelor's degree or higher in biomedical sciences, life sciences, computer science, or related field.
  • Minimum of 12 years of experience in clinical data management or related role in pharma/biotech/medical devices.
  • Significant leadership with 6-8 years of line management and building high-performing teams.

Responsibilities

  • Lead and mentor Data Management leaders, driving performance and development.
  • Ensure compliance with regulations (GCP), sponsor requirements, and Worldwide SOPs.
  • Oversee resource allocation and workforce planning for project support.
  • Monitor delivery, identify risks, and implement mitigation strategies.
  • Manage quality and issue processes, identify trends, and drive solutions.
  • Oversee budgets, profitability, and resource utilization across teams.
  • Collaborate with internal/external stakeholders for planning and risk management.
  • Lead development and continuous improvement of departmental processes and SOPs.
  • Guide Subject Matter Experts to ensure Data Management best practices.

Job description

Worldwide Clinical Trials, a global CRO, seeks an Associate Director of Clinical Data Management to lead data management strategy, operations, and quality across trials. You will drive compliance, resource planning, and timely delivery while shaping departmental processes and talent development.

You will collaborate with stakeholders across multiple time zones in a remote US-based role, ensuring high-quality data for clinical research and patient outcomes.

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