Setting the Standard: Performance, Quality, and Experience - These are the Hallmarks of Our Clinical Research Company. Discover Why We Stand Out from the Rest.
Therapeutic Experience
View Our List of Therapeutic Areas to See the Depth of Experience Our Clinical Research Company Brings to Your Study.
Cardiovascular Disease
Asthma
Hypertension
Obesity
Irritable Bowel Syndrome
Dementia
Women’s Health
COPD
Weight Loss
Ulcerative Colitis
Diabetes Mellitus
Vaccine
Osteoporosis
Hyperlipidemia
Osteoarthritis
Rheumatoid Arthritis
Alzheimer’s Disease
Migraines
Crohn's Disease
Anemia
We are committed.
Pioneer Clinical Studies understands that the key to any successful clinical trial is having reliable and accurate data entered in a timely fashion. We set high expectations for ourselves regarding the data that we provide to the Sponsors, and the care that we provide to our participants. We have several resources available to to help aid in the quality of our data collection.
We are quality.
We strive to provide every study participant with the best care. Our friendly, experienced, and knowledgeable staff members make sure that each patient is informed, comfortable, and satisfied with their involvement.
Accurate, accountable, and always working to be better, we ensure that protocols are executed correctly, deviations and errors are minimized, and all sponsor needs are met or exceeded timely and efficiently.
Medical advancements cannot take place without clinical research – be a part of the bigger picture.
Ensuring Data Integrity: Our Unwavering Commitment to Quality and Attention to Detail Vital for Successful Clinical Trials
Striving for Continual Improvement: Our Dedication to Progress and Growth
We perform internal study audits on a regular basis.
Review study protocols, EDC screen shots, and source documents to ensure that the source accurately and completely reflects the protocol’s requirements and site’s documentation requirements
Review completed source documents for accuracy, completeness, and legibility
Compare data in source documents to data transcribed in EDC for accuracy
Identify trends in errors to initiate improvements in source document flow, collection, and site processes
Review regulatory binders for proper organization, filing, delegation of authority, documentation, and completeness of training
Review site processes and forms and suggest revisions that will make the collection of data more streamlined
Adherence to these processes, in combination with FDA guidelines for research and good clinical practices is what leads PCS to constantly evolve, improve, and efficiently provide your company with quality data.
Discover Your Path to Better Health: Let Us Help You Find the Right Clinical Trial for You
Join the Movement, Make a Difference: Participate in Clinical Trials and Get Compensated for Your Time and Access Free Medical Procedures