Remote Associate Director, Clinical Data Management

Worldwide; Wilmington, Boston, Durham (DE, MA, NC); Ibrido; USD 119.000 - 236.000; Tempo pieno

Descrizione del lavoro

Worldwide Clinical Trials is seeking an Associate Director of Clinical Data Management for a remote role open to candidates based in the United States. You will lead data management teams, drive regulatory compliance, manage budgets, and partner with stakeholders to ensure timely, high-quality delivery across trials.

The role requires 12+ years in clinical data management with 6-8 years in leadership, strong communication skills, and strategic oversight of complex programs.

Competenze

• 12+ years of experience in clinical data management or a related role.
• 6-8 years of line management experience and developing high-performing teams.
• Expert knowledge of clinical data management practices, technologies, and regulatory expectations.

Mansioni

• Lead and mentor Data Management leaders, fostering team performance and development.
• Drive compliance with regulations, GCP, sponsor requirements and Worldwide SOPs.
• Oversee resource allocation and workforce planning for efficient project support.
• Monitor project delivery and mitigate risks to keep programs on track.
• Manage departmental quality and issue management processes; identify trends.
• Provide strategic oversight of budgets, profitability, and resource utilization.
• Partner with stakeholders for project planning, risk management and decision-making.
• Lead development and continuous improvement of departmental processes and SOPs.
• Guide SMEs and management to ensure consistent execution of best practices.

Conoscenze

Leadership

Data management

Budget management

Regulatory knowledge

Communication

English proficiency

Formazione

Bachelor's degree or higher

Descrizione del lavoro

Worldwide Clinical Trials is seeking an Associate Director of Clinical Data Management for a remote role open to candidates based in the United States. You will lead data management teams, drive regulatory compliance, manage budgets, and partner with stakeholders to ensure timely, high-quality delivery across trials.

The role requires 12+ years in clinical data management with 6-8 years in leadership, strong communication skills, and strategic oversight of complex programs.