Our clinical research services include:
- Single point of contact for budgets, contracts, regulatory and patient recruitment. Ability to execute Master Confidentiality Disclosure Agreement (MCDA), standardized budget and Master Clinical Trials Agreement (MCTA) with sponsors.
- Centralized processing of all aspects of clinical trials, including identifying diligent, well-trained investigators; recruiting, enrolling, and retaining study subjects; planning protocol strategies; preparing and submitting regulatory documents.
- Database of potential investigators, with quick investigator selection that can match study/trial needs with an appropriate physician(s).
- Large patient database to enroll an adequate number of study patients to meet study/trial needs; accomplished by patient database searches, referrals from partner medical practices, advertisements by research team.
- Experienced research team that includes a research director, administrative director, multiple clinical research coordinators, research associates, administrators, and support staff.
- Board-certified physicians in all the major medical and surgical specialties.
- Investigators with vast experience in conducting government and industry-sponsored research.
- Strong graduate medical education (GME) programs including residency training, medical students and other academic programs in multiple discipline.
- Support from highly skilled advanced practice nurses, registered nurses, licensed technologists in all fields, and dedicated ancillary and support staffs.
- Research administration committed to advancing medical and scientific knowledge.
- Ability to utilize sponsor selected central IRB. Also able to work with other central IRB’s, such as Western Institutional Review Board (WIRB) and IntegReview.
