About this role

Identify opportunities to optimize clinical trial processes across the study lifecycle
Lead cross-functional teams in the design, implementation, and sustainment of process improvements
Ensure site perspectives are represented in process redesign efforts
Assess current-state workflows, identify root causes of inefficiencies
Develop and monitor key performance indicators, dashboards, and reporting
Report progress, insights, and recommendations to executive leadership
Establish governance, documentation, and standard work
Build strong partnerships across clinical, operational, quality, technology, and site teams
Collaborate with sites, sponsors, contract research organizations, and vendors

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
Ability to establish relationships and develop strategic relationships within and outside of direct organization
Facilitation and communication skills
Process improvement skills and techniques
Change management skills and techniques
Excellent active listening skills
Ability to thrive in team environments of considerable change

Director, Clinical Trial Strategy – Optimization

Key skills