Adrienne Statti

Clinical Project Manager

Professional Overview

Adrienne Statti is an experienced Clinical Project Manager with a proven track record of driving the successful execution of complex clinical trials. With a strong background in clinical research and project management, she has developed expertise in coordinating multi-disciplinary teams, managing operational workflows, and ensuring regulatory compliance within the pharmaceutical and biotechnology industries.

Experience Summary

Current Role

As a Clinical Project Manager at CTI Clinical Trial and Consulting Services, Adrienne is responsible for overseeing the end-to-end delivery of clinical trial projects. She manages project timelines, budgets, and resources, while collaborating closely with cross-functional teams to mitigate risks and ensure the timely completion of study milestones. Adrienne's ability to leverage her clinical expertise and project management skills has enabled her to deliver high-quality results and contribute to the advancement of new therapies.

Career Progression

Prior to her current role, Adrienne held various positions at PAREXEL, where she gained extensive experience in clinical research and project management. She began as a Lab Tech, progressing to Clinical Laboratory Coordinator and then Clinical Research Coordinator, before transitioning into her current role as a Clinical Project Manager. Adrienne's diverse background and adaptability have been instrumental in her career growth, allowing her to take on increasingly complex responsibilities and contribute to the success of multiple clinical trial projects.

Academic Background

Adrienne holds a Bachelor's degree in Biology, which has provided her with a strong foundation in the scientific principles underlying clinical research. Her academic achievements, combined with her practical experience, have equipped her with the necessary skills and knowledge to excel in the pharmaceutical and biotechnology industries.

Areas of Expertise

• Clinical trial project management

• Operational workflow optimization

• Regulatory compliance and quality assurance

• Cross-functional team coordination

• Risk mitigation and issue resolution

• Stakeholder management and communication

Professional Impact

Throughout her career, Adrienne has made significant contributions to the advancement of clinical research. She has successfully managed the execution of multiple clinical trials, ensuring that projects are delivered on time, within budget, and in compliance with regulatory standards. Adrienne's ability to effectively navigate complex project environments and foster collaborative working relationships has been instrumental in the successful completion of these studies, ultimately supporting the development of new and innovative therapies.

Conclusion

Adrienne Statti is a dedicated and accomplished Clinical Project Manager with a proven track record of driving the successful execution of clinical trials. Her comprehensive experience, strong technical expertise, and collaborative leadership style position her as a valuable asset to any organization in the pharmaceutical and biotechnology industries.