Open to opportunities

Judith Udeke

@judithudeke1

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Accomplished Clinical Trial Manager with extensive international experience.

United States

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What I'm looking for

I am seeking a role that fosters collaboration, innovation, and professional growth in clinical research.

I am an accomplished Clinical Trial Manager with over 16 years of international experience in clinical research. My expertise lies in overseeing clinical trials from inception through to regulatory compliance and submission. I have a proven track record of driving high-performing cross-functional teams, optimizing clinical trial processes, and fostering strong vendor and stakeholder relationships.

Throughout my career, I have successfully reduced trial timelines, improved patient recruitment, and maintained compliance with regulatory standards across various therapeutic areas, including oncology, metabolic diseases, and vaccine development. I am passionate about continuous improvement and committed to delivering high-quality results in complex, fast-paced environments.

Experience

Work history, roles, and key accomplishments

Current

Senior Clinical Trial Manager

Current

Centene Healthcare

Oct 2022 - Present (2 years 9 months)

Developed and executed risk-based monitoring strategies that reduced site deviations by 30% and improved data integrity. Led clinical trial site selection and feasibility assessments, reducing trial startup timelines by 20%.

Risk Based Monitoring Feasibility Assessment Regulatory Compliance Vendor Management Patient Recruitment Data Management ICH GCP

Senior Clinical Trial Manager

ICON Clinical Research Service

Mar 2021 - Oct 2022 (1 year 7 months)

Managed the planning, execution, and closeout of clinical trials across multiple therapeutic areas, achieving study milestones on time and within budget. Supervised project budgets of $1M to $5M per trial, consistently tracking expenditures and ensuring cost-effective trial management.

Clinical Trial Management Budget Management Risk Assessment Client Communication Regulatory Submissions Project Planning

Clinical Research Manager

Synteract (A Syneos Health Company)

Feb 2019 - Mar 2021 (2 years 1 month)

Coordinated clinical trials, ensuring adherence to timelines, budgets, and regulatory requirements. Managed study site selection, initiation, and monitoring, ensuring quality data collection and patient safety.

Site management Budget Management Regulatory Compliance Cross Functional Team Leadership Regulatory Submissions

Clinical Team Lead

Covance USA

Jan 2016 - Feb 2019 (3 years 1 month)

Managed cross-functional clinical teams for Phase I-IV clinical trials, ensuring adherence to regulatory guidelines. Reduced study-related risks by 25% through proactive risk management strategies and process improvements.

Risk Management Regulatory Compliance Training And Development

Senior Clinical Research Associate

Chiltern USA

Apr 2014 - Jan 2016 (1 year 9 months)

Managed clinical trial activities from initiation through completion, ensuring protocol compliance and patient safety. Trained and mentored junior CRAs, enhancing team performance and reducing turnover by 15%.

Compliance Patient Safety Mentoring Junior CRAs Cross Functional Collaboration

Clinical Research Associate

Theorem Clinical

Mar 2011 - Apr 2014 (3 years 1 month)

Coordinated site visits, ensuring adherence to study protocols and regulatory requirements. Managed patient recruitment strategies, achieving 85%–90% enrollment targets within study timelines.

Regulatory Compliance Patient Recruitment Regulatory Submissions Enrollment Targets

Education

Degrees, certifications, and relevant coursework

Louisiana State University

Bachelor of Science, Chemical Engineering

Studied Chemical Engineering at Louisiana State University. Gained foundational knowledge in chemical processes and engineering principles relevant to various industries.