We understands that clinical trials are vital to advancing medical knowledge and treatment. At Proficient Clinical Research, we match our clinical research experience with superior quality, clinical innovation, quality, and dedicated care. Our staff has over 10 years of clinical research experience and is strategically connected within the clinical research/pharmaceutical industry.
Our unique business model allows us to negotiate a single contract and budget for multiple sites selected on a single protocol. This drastically cuts down the negotiation and start-up time for the sponsor, and gives our sites more time than competitors to enroll patients. Additionally, we cooperate as a group to share resources like source documentation which further cuts down on our individual site start-up timelines.
We play by the numbers: more sites equates to more patients, particularly when sites are working together towards the same goal.
Give your current patients access to novel treatment options and expand your practice and reputation by taking part in ongoing cutting-edge research. Chase your scientific interests and potentially be part of the next breakthrough, all while earning additional compensation for seeing patients you already regularly treat in your practice.
Proficient Clinical Research provides clinical operations and consulting services to Pharmaceutical, Biotechnology, and Medical Device companies, as well as Contract Research Organizations (CROs) and Healthcare Professionals. Our aim is to accelerate the delivery of innovative treatments to patients by guiding them through the clinical trial process. We partner with private practice physicians and healthcare groups to facilitate their patients’ access to clinical research opportunities. Furthermore, we offer comprehensive clinical trial monitoring and site management services, enabling healthcare professionals to expand their practice without being burdened by administrative challenges.
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