Head of Clinical Program Delivery & Planning

DM Clinical Research; Houston (TX); On-site; USD 150,000 - 230,000; Full time

Job summary

DM Clinical Research in Houston, TX seeks a Director of Program Management and Planning to lead PMO operations for clinical programs and drive strategic planning. You will oversee cross-functional teams, interface with executives, and serve as the primary sponsor/CRO contact on key trials.

The role requires 8+ years in project management, with clinical trial experience and PMP certification preferred. You will develop PM processes, mentor staff, and ensure on-time study milestones and enrollment

Qualifications

• Education: Bachelor’s Degree required, Master’s Degree preferred.
• Experience: 8+ years in project management; Clinical Trial Management experience preferred.
• Credentials: PMP certification preferred.
• Knowledge/Skills: strategic thinking, leadership, communication, diplomacy, and problem-solving.

Responsibilities

• Direct PM operations and strategic planning to meet organizational goals.
• Develop and govern PM processes, dashboards, templates, policies, and metrics.
• Monitor projects, anticipate roadblocks, and provide clear status updates to executives and stakeholders.
• Lead cross-functional, sponsor/CRO communications and manage government project deliverables.
• Coach PM staff and report on PM KPIs for continuous improvement.
• Act as key client contact for designated clinical programs and drive enrollment and data quality.

Skills

Leadership

Stakeholder management

Cross-functional collaboration

Strategic planning

Project management

Communication

Mentoring

Problem-solving

Risk management

Reporting

Education

Bachelor's Degree

Master's Degree preferred

Job description

DM Clinical Research in Houston, TX seeks a Director of Program Management and Planning to lead PMO operations for clinical programs and drive strategic planning. You will oversee cross-functional teams, interface with executives, and serve as the primary sponsor/CRO contact on key trials.

The role requires 8+ years in project management, with clinical trial experience and PMP certification preferred. You will develop PM processes, mentor staff, and ensure on-time study milestones and enrollment