A Dedicated and Agile Team

Wakefield Clinical Research is led by a team of experienced clinical research professionals dedicated to supporting innovative biotechnology, pharmaceutical, and medical device companies.

Our team brings expertise in clinical trial design, regulatory strategy, project management, and clinical study execution. Through our integrated CRO and clinical research site model, we provide sponsors with direct access to experienced professionals who are actively involved in each stage of the study.

 ✔ Direct communication with experienced clinical professionals
✔ Hands-on operational oversight for every study
✔ Flexible support tailored to emerging biotech sponsors
✔ Integrated CRO and clinical trial site collaboration
✔ Efficient decision-making and streamlined communication  

 Dr. Hodgkins has extensive experience in clinical research operations, regulatory strategy, and early-phase clinical study management. She has worked with biotechnology and pharmaceutical sponsors to design and execute clinical trials across multiple therapeutic areas.

Her leadership focuses on building an integrated CRO and clinical research site model that enables efficient study startup, strong regulatory compliance, and high-quality clinical data.

• Clinical project management
• Clinical monitoring (CRA)
• Study coordination
• Regulatory submissions and IRB management
• Data management and study documentation

Our team works closely with sponsors to ensure that clinical trials are conducted according to protocol, regulatory requirements, and Good Clinical Practice (GCP).

Our clinical site team includes:

• Principal investigators and sub-investigators
• Study coordinators
• Clinical research nurses
• Laboratory and PK sampling staff

This integrated structure enables efficient study execution and high-quality data collection.

 Unlike large CROs where projects may be transferred across multiple departments, sponsors working with Wakefield interact directly with experienced professionals responsible for study execution.

This structure enables:

✔ Faster decision-making
✔ Clear communication
✔ Direct operational oversight
✔ Strong accountability

 Wakefield Clinical Research collaborates with external specialists, investigators, and clinical experts when needed to support specific study requirements. This flexible model allows us to provide sponsors with the expertise required for complex clinical development programs.