Clinical R&D
CRO Liaison
Omar Consulting Group partners with multiple clinical research organizations (CROs) for clinical services. Omar is constantly watching the horizon for CROS with subspecialties in areas of therapeutic interest and special patient populations.
Site Selection and Qualification
Site selection and qualification is a science. Sites are selected based on the investigator’s skill, access to patients, and willingness to do work according to a written protocol. Additional items such as equipment, staff, and favorable standing with the FDA (no debarments) are essential elements in selecting and qualifying a site.
Clinical Study
Clinical studies may be run and managed by individual investigators, or clinical research organizations (CROs).
Operations
Omar Consultants will help you oversee the operations of your trial:
- Preparation for and attendance at kick off meetings
- Preparation for and attendance at Investigator’s meetings
- Attendance at operations team meetings
- Interim monitoring visits
- Close Out monitoring visits
Forensic Auditing of Trials
On site forensic monitoring (after database lock) of specific sites.
Database Lock
A secondary review of trial master files is provided in order to facilitate database lock.
Content Development Services
Content development for a variety of regulatory, clinical, and strategic medical communications.