The mission of Pharma Care Research is to contribute to the development of pharmaceutical products and medical devices through the quality performance of clinical trials and to improve the health of individuals in our global community. We partner with research sponsors with the goal of consistently fulfilling enrollment expectations, providing high quality data, and demonstrating excellence in efficiency and professionalism. Pharma Care Research is a place where life, the individual and the family are nurtured and respected. Through education we empower people to more effectively care for themselves and those for whom they care. With an emphasis on service, and by providing the highest quality up to date medical care, we strive to help all people achieve their full potential at every stage of life.
Our professional, multi-lingual staff bring many years of interdisciplinary expertise together to provide well-coordinated support to our investigators and high-quality services to our sponsors. Pharma Care Research adheres to the International Conference on Harmonization (ICH) and Good Clinical Practice (GCP). GCP guidelines are in place to protect our patient’s rights as a volunteer in a research trial. GCP guidelines also define the responsibilities of study sponsors (i.e. pharmaceutical companies) and research physicians and coordinators. We are also observant of the protection of patients in our clinical research studies and Health Insurance Portability and Accountability Act (HIPAA) compliant.
All Pharma care Research clinical staff members are certified in Basic Life Support (BLS) and/or Advanced Clinical Life Support (ACLS). Through their training in these areas, our staff readily recognizes adverse reactions and is quick to respond to these situations if they occur. Stringent safety precautions are always taken as we care for our patients.
Our staff consists of 9 physician principal and sub-investigators with a minimum of 10 years in Phase I-IV trials, four full-time clinical research coordinators; three certified by the Association of Clinical Research Professionals, two full-time A.R.N.P sub-investigators, a registered dietitian, a certified PharmD, IATA certified full-time phlebotomists, regulatory specialists and a full-time recruiter
At Pharma Care Research, we know that cost and timelines are critical concerns. All aspects of your study are dealt with in a timely, professional manner. Contracts and Budgets have a 1 week turn-around. We are able to work with the Central IRB of your choice.