Why we're the Leaders in Clinical Research

Omega Research Consultants is a premier research organization with several locations
throughout the Central Florida and coastal Florida regions. Built on the foundations
of Compassion, for our study patients, Excellence, for our trial sponsors and partners,
and Integrity, by building strong relationships through honesty, openness and professionalism,
Omega Research Consultants is quickly becoming a known leader in clinical trial operations.

Our size and locations allow us the unique opportunity to perform in a wide arrange of
clinical arenas while still maintaining that personal touch that is often missing in large
corporations. From the initial contact to site close out, we are committed to providing
outstanding service that delivers timely and accurate data, well-qualified participants, low
lost-to-follow-up ratios and personalized attention to ensure the success of the trial. Adherence
and compliance with international standards of Good Clinical Practice (GCP) and International
Conference of Harmonization (ICH) are the foundation of our quality systems.

Omega Research Consultants has access to a vast array of patient databases to ensure timely
enrollment. Omega also contracts with many local practitioners well known for their practices
in endocrinology, nephrology, gynecology, rheumatology and internal medicine, to name just a few.
This allows for quicker and more accurate patient recruitment.

In house, Omega Research Consultants is supported by a close team of doctors, nurses and other
health professionals who take pride in making every single interaction positive, every single time.
Our study sites boast a warm, inviting atmosphere with large exam-rooms and cozy infusion rooms to
ensure patient comfort. For our professional associates, we offer generous monitoring space, copy and fax capabilities as well as complimentary Wi-Fi.

Quick Facts

  • • Established 2006
  • • Over 200 years of combined research experience
  • • Database of over 7500 active patients
  • • Experience in conducting Phase I through Phase IV trials
  • • Dedicated Phase I site able to host 24 number of subjects at one time
  • • Lost to follow up rate less than 2% due to rigorous prescreen methods
  • • Dedicated site staff including:
  •         o Full-time Regulatory Specialists
  •         o Budget/Contract Department
  •         o ACLS Certified Registered Nurses, Practical Nurses and Medical Assistants experienced in phlebotomy
  •         o Onsite PI/Sub-I to ensure subject safety
  • • Spacious Infusion Room with seating for 8 subjects at once
  • • plus more