Integrity. Responsiveness. Quality. Accuracy.
Our services include Site Monitoring, Site Management, Project Management, Data Management, Medical Writing, Pharmacovigilance and Statistical Support. We also provide staffing services to include Clinical Trial Assistants and site based Study Coordinators.
We are able to meet all the clinical needs of a single site phase I trial through a large multi-center phase III project.
Our team includes employees and regional based clinical research consultants, to allow flexibility in meeting sponsor needs. Each member of the CUREM Research Partners team has been individually chosen by the CEO and principal consultant based on a prior working relationship.
Our focus is prioritizing and putting processes in place to achieve the aims of your project. We carefully plan and track the monitoring and action items necessary to provide an accurate assessment of your study.
Each member of our team possesses the attritbutes of integrity, dedication, personal commitment, responsiveness, professionalism and attention to detail.
We believe that the phrase 'Dotting the I's and crossing the T's' is not a cliché but the only way to do business in this industry. After all, the only way to bring safe and reliable drugs to the market that will help people is through integrity, responsiveness, quality and accuracy.
To find out how our company can help you achieve your goals, call 734-253-2632 today. Or, email us at info@curemresearch.com.