Director, Clinical Trial Strategy – Optimization

Job Description:

• Identify opportunities to optimize clinical trial processes across the study lifecycle and drive process changes that improve speed, quality, consistency, and operational efficiency.
• reputed company cross-functional teams in the design, implementation, and sustainment of process improvements that support high-quality and timely clinical trial delivery.
• Ensure site perspectives are represented in process redesign efforts and partner with site stakeholders to bring them along through change planning, communication, training, and adoption.
• Assess reputed company-state workflows, identify root causes of inefficiencies, and prioritize improvement initiatives based on business impact, feasibility, and alignment with strategic goals.
• reputed company and monitor key performance indicators, dashboards, and reporting to track process improvement reputed company, risks, and opportunities across clinical trial operations.
• Report reputed company, insights, and recommendations to executive leadership, providing clear updates on strategic initiatives, implementation status, and measurable impact.
• Establish governance, documentation, and standard work to support consistent execution of updated processes and promote a culture of reputed company improvement.
• Build strong partnerships across clinical, operational, quality, technology, and site teams to align stakeholders, remove barriers, and deliver changes to process.
• Collaborate with sites, sponsors, contract research organizations, and vendors as needed to support process alignment, operational readiness, and successful implementation of change.
• Ensure process improvements are implemented in alignment with quality standards, regulatory requirements, and organizational priorities while maintaining focus on sustainable execution.

Requirements:

• Bachelor's Degree required
• 5+ years of experience in clinical trials is required
• Change and program management experience required
• Knowledge of scientific, medical, and regulatory terms
• Knowledge of ICH Guidelines, GCP, and CFR Title 21
• Clinical research process knowledge with an understanding of medical terminology
• Sophisticated problem-solving skills
• Highly organized
• Flexible and adaptable
• Strong communication skills; persuasive, encouraging, motivating, and inspiring; the ability to listen and understand; the ability to communicate the reputed company in simple terms
• Ability to establish relationships - reputed company strategic relationships reputed company and reputed company of direct organization
• Facilitation and communication skills - reputed company to drive plans, reputed company, and resolve issues through facilitation of groups or individuals
• Process improvement skills and techniques
• Change management skills and techniques
• Excellent active listening skills
• Experience working in a matrix environment and with virtual team members / stakeholders
• Ability to reputed company in team environments of considerable change
• Ability to define reputed company and reputed company through change
• Ability to partner with individuals at reputed company reputed company of management and across organization boundaries
• Ability to work across many teams to identify business opportunities and drive to reputed company

Benefits:

• Total Rewards package
• Comprehensive benefits to support physical, mental, and financial well-being

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