Our counselling and clinical trials team is united by a shared commitment to improving patient outcomes and advancing medical knowledge. We collaborate by integrating clinical expertise with compassionate support, ensuring that every participant feels valued and cared for throughout the research process. This synergy not only enhances the quality of our trials but also fosters an environment of trust and understanding, ultimately driving us toward our common goal of effective and innovative healthcare solutions.
Prevention & Strengthening Solutions was founded in December 1998 by Dr. Mark Smikle with Prevention in mind to assist people in the prevention of the development of anxiety/phobia (maladaptive coping), and to be a positive resource in the community to strengthen self-confidence and problem-solving in dealing with life’s stressors.
Dr. Smikle earned his undergraduate degree in Psychology from Columbia College, his Master's degree in Public Health at Austin Peay State University, and his Doctorate in Clinical Psychology from California Coast University.
His experience includes working in a Mental Health Hospital and counseling troubled teenagers and their families in residential facilities and their homes.
He has been counseling in clinical research settings, and now in his private practice.
Our counseling and clinical trials team is built on a collaborative and supportive culture where empathy, respect, and open communication guide everything we do. We work closely together, sharing knowledge and clinical insight to strengthen patient care and improve research outcomes.
We are committed to continuous learning and professional growth, ensuring our team remains current with evolving methodologies, therapeutic approaches, and advancements in clinical research. This research-driven environment empowers every team member to contribute meaningfully to both patient well-being and the advancement of clinical science.
CLINICAL RESEARCH SKILLS:
Study Site Management, Study Drug Management, and Study Start-up & Close-out Activities.
Clinical Trial Budget & Contract Negotiation also participated in Sponsor & Investigator/Initiation Meetings.
Serve as the Site CRA (In-House Monitor) for a Clinical Research Site.
Ensured that the Study Site’s Regulatory Documents (1572s, IRB Informed Consents, IRB Approval Letters, Protocols, Financial Disclosures, SOPs, Continuing Reviews, etc.) were completed and current throughout the Study Trial.
Work with Sponsors, CROs, Central IRBs, & Research Team Members.
Lead Study/Regulatory Coordinator for CNS & Diabetes Clinical Trials.
Subject Recruitment, Subject Source & CRF Documentation & Completion, AEs/SAEs Reporting, & Data Abstraction & Data Management.
Patient care duties: Review & Consenting of Subjects, vital signs, blood & tissue specimen collection, ECG, injections, subject diaries, patient questionnaires, Study Source & CRF Query resolutions, scheduled Subject Study appointments per the Protocol timelines, & Subject/Patient Education.
Kaplan University Business Administration (BA), Marketing
Plan, develop, organize, implement, direct & evaluate the organization’s fiscal function & performance.
Participate in developing the corporation’s plans & programs as a strategic partner.
Develop credibility for the finance group by providing timely and accurate analysis of budgets, financial reports & financial trends.
Enhance /or develop, implement & enforce policies & procedures of the organization by way of systems that will improve the overall operation & effectiveness of the corporation.
Establish credibility throughout the organization & with the Board as an effective developer of solutions to business challenges.
TUI University
CLINICAL RESEARCH SKILLS:
Study Site Management, Study Drug Management, Study Start-up & Close-out Activities.
Clinical Trial Budget & Contract Negotiation also participated in Sponsor & Investigator/Initiation Meetings.
Served as the Site CRA (In-House Monitor) for Clinical Research Sites.
Ensured that the Study Site’s Regulatory Documents (1572’s, IRB Informed Consents, IRB Approval Letters, Protocols, Financial Disclosures, SOPs, Continuing Reviews, etc.) are completed and current throughout the duration of the Study Trial.
Worked with Sponsors, CROs, Central/Local IRBs, & Research Team Members.
Lead Study/Regulatory Coordinator & Research Nurse for Neurology & Oncology Clinical Trials.
Subject Recruitment, Subject Source & CRF Documentation & Completion, AEs/SAEs Reporting, & Data Abstraction & Data Management.
Patient care duties: Review & Consenting of Subjects, vital signs, blood & tissue specimen collection, ECG, injections, subject diaries, patient questionnaires, Study Source & CRF Query resolutions, scheduled Subject Study appointments per the Protocol timelines, & Subject/Patient Education.
After graduating from High School, Marlon pursued his Bachelor of Business Administration with a focus in Finance and a Business Law minor at Stetson University in Deland, Florida.
Shortly after receiving his Bachelor's degree and working in the finance industry, Marlon relocated to Valparaiso, Indiana, and received his Juris Doctor from Valparaiso University School of Law.