Strategic Program Director: PM & Planning Excellence

Dm Clinical Research Group; Houston (TX); On-site; USD 160,000 - 220,000; Full time

Job summary

Dm Clinical Research Group in Houston, TX seeks a Director of Program Management and Planning to lead and direct project management operations and strategic planning for multiple clinical trial programs. You will shepherd relationships with external stakeholders and drive organizational goals through robust PM processes and governance.

The role requires 8+ years in project management within the clinical trials space, a PMP background is preferred, and experience coordinating with CROs and pharma

Qualifications

• Bachelor’s degree required; Master’s preferred.
• 8+ years of project management experience in clinical trials; CRO/pharma exposure at senior level.
• PMP certification preferred.
• Strong leadership, communication and stakeholder management skills.
• Experience interfacing with CROs and pharma partners.

Responsibilities

• Develop, implement, and govern program management processes, dashboards, templates, policies, and metrics.
• Drive expedited study startup and oversight of key clinical trial projects.
• Serve as the primary client sponsor/CRO contact and build relationships to drive business.
• Coach and mentor PM staff and monitor enrollment and data quality metrics.
• Provide guidance on scope, risk mitigation, resource planning and deliverables.

Skills

Leadership

Communication

Strategic thinking

Problem solving

Organizational skills

Diplomacy

Education

Bachelor’s Degree

Master’s Degree preferred

Job description

Dm Clinical Research Group in Houston, TX seeks a Director of Program Management and Planning to lead and direct project management operations and strategic planning for multiple clinical trial programs. You will shepherd relationships with external stakeholders and drive organizational goals through robust PM processes and governance.

The role requires 8+ years in project management within the clinical trials space, a PMP background is preferred, and experience coordinating with CROs and pharma