QARA provides expert clinical trial operations services to the pharmaceutical and biotechnology industry. Our consultants are experienced in study feasibility, clinical trial management, clinical monitoring, expedited study initiation, and patient recruitment strategy. QARA provides professional and regulatory compliant services to ensure clinical development occurs on-time and within your cost objectives.

Study Feasibility

Our feasibility assessment team will provide, detailed feedback from clinical research sites including patient enrollment rate, number of sites needed, local standard of care, viable patient assessments, potential study challenges, and investigator grants. We can provide the specific site feedback needed to make important study decisions up-front.


Clinical Trial Management

Our clinical study managers will map out operational objectives impacting time, cost, and quality outcome for your clinical development program. They will monitor and ensure trials remain well planned and executed throughout their life cycle.  Areas of expertise include efficient start-up; patient recruitment; best clinical practice for trial operations; and strong clinical research associate (CRA) leadership and oversight.


Patient Recruitment

QARA provides a proactive approach and strategic enrollment plan that is data driven and site specific. Our professional team can work directly with your sites and maximizing qualified patient recruitment in the shortest time possible.


Clinical Monitoring

Our CRAs are professional, articulate, and thorough.  They are experienced at establishing effective working‑relationships with sites to ensure patient recruitment and study execution goals are met.  QARA clinical monitoring services include traditional, full-service monitoring, as well as risk-based and centralized monitoring services, with regional CRAs available for assignment to your project.