Our Team

CUREM employs highly experienced clinical research consultants and employees that have been individually chosen by the CEO and principal consultant based on prior working relationships. Key attributes shared by each team member are integrity, dedication, personal commitment, responsiveness, professionalism and attention to detail. 

We are comprised of regionally based colleagues/contractors throughout the US in roles of: site monitoring, data management, clinical trial administration, regulatory support, study coordination, safety monitoring, medical monitoring and biostatistics.

Clincal Operations

Wendy Eggleston CUREM Research Partners Clinical Operations are headed by founder and principal consultant, Wendy Eggleston.  Wendy has 20 years of industry experience with a large pharmaceutical company, a biotechnology company and a Clinical Research Organization.

As a Clinical Research Associate and Clinical Scientist at Parke-Davis/Pfizer for 7 years, Wendy worked in the Cardiovascular Clinical Research Department and assisted Lipitor to a NDA.  She furthered her research in hypercholesterolemia at Esperion Therapeutics and managed the proof of concept trial in A1-Milano for reverse cholesterol transport which finished with statistically significant results.  

Wendy has worked for a Clinical Research Organization as the Director of Clinical Operations. In this position Wendy was responsible for overseeing the project management, medical writing and monitoring staff. She was involved in creating SOPs, training procedures, and business/bid development.

Wendy’s education includes a M.S. degree from the University of Michigan in Clinical Research Design and Statistical Analysis, a B.S. in Communications and an A.S. in Cardiovascular Technology.   

At CUREM Research Partners, Wendy leads a strong clinical team of Project Managers, Medical Writers and Clinical Research Associates. The majority of monitors have over 10 years experience across a broad range of clinical practices and therapeutic areas. Nearly 80% of the CRAs are registered nurses and all are experienced with electronic data capture. Our monitors are regionally based which facilitates efficiencies with travel costs and results in a positive effect on enrollment due to close relationships with clinical sites. 

Our medical writer is a field expert bringing 20 years experience writing for both pharmaceutical and biotechnology companies. 

Technical Operations

CUREM has an experienced staff of technical experts experienced in all aspects of trial execution. Our Lead Data Manager has over 13 years of clinical experience in the roles of data manager, clinical monitor and study manager. She has worked for 4 years at Parke-Davis/Pfizer as a data manager and 2 years at Phase Forward as a manager in clinical trial design and application engineering. She has also held positions in monitoring and study management which gives her a full picture understanding of all roles.

Our clinical research partners team of data managers has an average of 8 years experience in both paper and electronic system data capture systems.

Our lead biostatistician is a leading-edge expert in experimental design, protocol development and statistical analysis with 20 years experience as a statistician and associate director at Park-Davis/Pfizer.


CUREM has clinical trial assistants available who are experienced with study start up activities, regulatory document review, electronic trial master files and assisting the CRA and Project Management teams to meet goals. 


CUREM Research Partners provides complete SAE reporting services and medical monitoring by our pharmacovigilance team.  Our drug safety specialist has 12 years experience in drug safety at large pharmaceutical companies. Our medical monitor has worked as a medical director within the industry and brings 10 years of experience.  


Our Lead QA/GCP Regulatory Compliance Auditor has 16 years experience conducting audits of clinical research trial sites, sponsor master files, and vendor qualification audits. He also has 12 years of international trial experience throughout Latin America.    

To find out how our company can help you achieve your goals, call 734-253-2632 today. Or, email us at info@curemresearch.com.