About Us
Who We Are
Equity Clinical Solutions has been involved in clinical research since 1993. We have worked with various pharmaceutical, biotechnology, medical device, and clinical research organizations (CROs). We have assisted in the development and implementation of clinical research audits, protocols development from concept to phase IV, and post marketing trials. We specialize in the strategic development,
management and analysis of programs that support Clinical Research Operations.
We are Equity Clinical Solutions, a Limited Liability Corporation, whose mission is to create healthcare opportunities for all and alleviate healthcare disparities that currently exist, particularly in the underrepresented and underserved communities.
Our vision is simple, we aim to collaborate with healthcare community outreach programs and build relations where people are empowered to participate in clinical research.
Healthcare disparities are a crucial aspect of public health and healthcare policy to ensure that all individuals have equitable access to healthcare services and the opportunity to achieve good health regardless of their background or circumstances. Efforts to reduce healthcare disparities often involve improving access to care, increasing healthcare provider cultural competence, and addressing systematic inequalities in healthcare systems.
Meet The Team
Pamela Shelton
With 30 years in the Research and Development arena, Pamela has worked as a Clinical Assistant, Regulatory Affairs Associate, Clinical Research Associate, Trainer and GCP Compliance Auditor. The last 15 years have been spent consulting with Contract Research Organizations and sponsor companies as a GCP and GMP Compliance Auditor and/or Clinical Research Consultant. She has also worked with new clinical investigators to introduce them to the world of Clinical Research. Pam’s extensive experience in GxP and knowledge of FDA and EMA regulations ensures she provides expert consulting services. She is a member of the Women of Color in Pharma, Drug Information Association, and Society of Quality Assurance. Pam currently resides in Atlanta, GA, and enjoys riding her Peloton and wardrobe editing for family and friends in her spare time.
Skilled Certified Clinical Research Associate (CCRA) with over a 24 year plus track record of success in progressively responsible positions in clinical trial environments with pharmaceutical, Biotech, medical device companies, and medical sales. Experience in monitoring multiple protocols, site locations, evaluation, initiation, maintenance, and close-out visits in accordance with the protocol, ICH/GCP guidelines, government agencies, and company SOP’s, while ensuring integrity of study data and following study timelines. Extensive experience in training, mentoring, management, clinical study report writing, document preparation/submission to the FDA and/or ROW government agencies.
Calystia L. Wilkerson
Skilled Certified Clinical Research Associate (CCRA) with over a 24 year plus track record of success in progressively responsible positions in clinical trial environments with pharmaceutical, Biotech, medical device companies, and medical sales. Experience in monitoring and auditing multiple protocols, site locations, evaluation, initiation, maintenance, and close-out visits in accordance with the protocol, ICH/GCP guidelines, government agencies, and company SOP’s, while ensuring integrity of study data and following study timelines. Extensive experience in training, mentoring, management, clinical study report writing, document preparation/submission to the FDA and/or ROW government agencies.
Resume
Skilled Certified Clinical Research Associate (CCRA) with over a 24 year plus track record of success in progressively responsible positions in clinical trial environments with pharmaceutical, Biotech, medical device companies, and medical sales. Experience in monitoring multiple protocols, site locations, evaluation, initiation, maintenance, and close-out visits in accordance with the protocol, ICH/GCP guidelines, government agencies, and company SOP’s, while ensuring integrity of study data and following study timelines. Extensive experience in training, mentoring, management, clinical study report writing, document preparation/submission to the FDA and/or ROW government agencies.