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Years of Clinical Trial Experience
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Dr. Pollak has experience conducting trials across numerous indications including bunionectomy, hernia repair, total knee replacement, abdominoplasty, COVID-19, flu, and C. Difficile vaccines, tinea pedis, soft tissue infections, osteomyelitis, diabetic peripheral neuropathy (DPN), diabetic foot ulcers, devices, and more.

Dr. Pollak aims to match excellent research sites with outstanding sponsors and CROs.

Meet Dr. Pollak

Dr. Pollak has over 30 years of research experience and has been the principal investigator (PI) of over 200 clinical trials, including over 30 bunionectomy trials. Dr. Pollak has overseen multiple surgical studies, including abdominoplasty, hernia repair, and total knee replacement. He was also a key opinion leader (KOL) in onychomycosis for 15 years.

Early in his research career it became apparent to Dr. Pollak that to optimize the likelihood of a new drug obtaining approval by the FDA, there must be competent research sites and these sites must perform the trials in a timely manner. The quality of the site’s work is paramount to meeting the sponsor’s expectation of enrollment. The eternal truism is simple: “Under promise and over deliver”. The feasibility forms must be 100% realistic in terms of the site’s ability to carry out the trial. Too many trials have sites that either do not enroll a single patient or only enroll a few patients.

Dr. Pollak believes it is important to evaluate a clinical trial site thoroughly to ensure that they will be successful when accepting a clinical trial. It is also important for a site to say no to a sponsor if they are not confident that the trial is a good fit, and the expected enrollment cannot be met.

Dr Richard Pollak Bio picture

Dr. Pollak is a leading expert in bunionectomy clinical trials.

Dr. Pollak's Experience

Dr. Pollak attended the University of Massachusetts in Amherst, Mass. He graduated college in 1973 Cum Laude and later moved to San Francisco, California to attend California College of Podiatric Medicine and graduated Cum Laude in 1977.

He completed a 2-year podiatric surgical residency in Northlake, Illinois and obtained a Master of Science degree from the Pennsylvania College of Podiatric Medicine. He moved to San Antonio, Texas in 1979 and started the San Antonio Podiatry Associates where he was president of the group for nearly 40 years.

He started getting involved in clinical research from his podiatry office over 30 years ago. During this time, Dr. Pollak was president of Endeavor Clinical Research until his company was acquired by Evolution Research Group (ERG) in 2017. In September of 2022, he retired from ERG and now serves as president of Pollak Clinical Research Consulting LLC.

Services

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Our Expertise

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Sponsors

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Our Services

Consulting, Advising, & Business Development

We help match excellent sites with clinical trials that fit their strengths, helping to create mutually beneficial relationships between sites and sponsors.

Collaboration

We work to create collaboration among sites to reduce costs, create efficiencies, and save time.

Affiliations

We have created relationships with experts in regulatory, budgeting, contracts, study-startup, source documents, and patient recruitment.

Reasonable costs

By creating efficiencies across our site partners, we save you money. Get in Touch to find out more about our services or to request a quote.
Participate in a Study in San Antonio, TX - Participant Info - study coordinator with clinical study patient
Participant Info - study coordinator with clinical study patient

Benefits of Working with a Research Consultant

Along with Dr. Pollak’s extensive experience in the industry, he has also teamed up with leading experts to provide services for budgeting, clinical research agreements, regulatory, contracts, and patient recruitment. He also collaborates with experts who provide nearly identical source documents, budgets, and SOP’s.

Forming a high-quality selection of sites for a given trial streamlines the efficiency of both the CROs and sponsors, making the process extremely cost-effective. Implementing similar source documents and a single budget for multiple sites also results in cost savings for sponsors, CROs, as well as monitors.

Sponsors & CROs

Who Dr. Pollak has worked with:

Sponsors

CROs

Case Studies

Case Study

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Case Study

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Case Study

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