Jorge L. Sotomayor
Chief Executive Officer
Jorge L. Sotomayor leads Crown Research strategic growth, business development, and operational excellence in clinical research. He has a strong commitment to advancing medical innovation, working closely with investigators, healthcare providers, sponsors, and CROs to expand access to high-quality clinical trials and bring new treatment opportunities to patients.
Under his leadership, Crown Research has established a patient-centered approach focused on quality, compliance, and efficient study execution across multiple therapeutic areas, including Neurology, Pediatric Neurology, Psychiatry, Rheumatology, Nephrology, and Primary Care. Jorge is dedicated to building strong partnerships within the clinical research industry while fostering a culture of collaboration, integrity, and excellence.
His expertise in site development, strategic planning, and sponsor relations has contributed to the continued growth of the organization and its ability to successfully support a diverse portfolio of clinical studies. Jorge is passionate about connecting innovative research with the communities that need it most, helping advance healthcare through scientific discovery and patient participation.
Through his vision and leadership, Crown Research continues to strengthen its position as a trusted clinical research partner, committed to delivering exceptional results for sponsors, CROs, investigators, and patients alike.
Harold Tirado
Business Development & Operations Director
Harold Tirado plays a key role in driving organizational growth, strategic partnerships, and operational performance. With extensive experience in clinical research site development and business operations, he is responsible for identifying new opportunities, strengthening relationships with sponsors and CROs, and supporting the successful execution of clinical research programs.
His expertise spans site operations, feasibility assessments, patient recruitment strategies, and study startup activities, ensuring that projects are executed efficiently while maintaining the highest standards of quality and regulatory compliance. Harold works closely with investigators, healthcare providers, and research teams to create effective solutions that support both study objectives and patient needs.
Dedicated to advancing clinical research, Harold is committed to building long-term partnerships and expanding access to innovative therapies through well-managed and patient-focused clinical trials. His collaborative approach, operational leadership, and focus on continuous improvement contribute significantly to Crown Research's mission of delivering excellence in clinical research.
Through his leadership in business development and operations, Harold helps position Crown Research as a trusted partner for sponsors, CROs, and healthcare organizations seeking high-quality clinical trial execution and exceptional patient engagement.
research team
Jorge Sotomayor, MBA
Manager / Lead CRC
Clinical Research Manager with extensive experience in clinical trial operations, participant recruitment, study coordination, regulatory compliance, and site management. Experienced in overseeing study workflows, supporting investigators, coordinating sponsor communications, and ensuring high-quality execution of clinical research activities. Trained in ICH-GCP, human subject protection, regulatory compliance, and clinical trial operations.
Areas of Expertise
Clinical Trial Operations | Participant Recruitment & Retention | Study Visit Coordination | Regulatory Documentation | EDC Data Management | Protocol Compliance | Laboratory & Specimen Logistics | Biological Sample Shipping | Sponsor & CRO Communication | Site Operations Management | Human Subject Protection | Quality Assurance & GCP Compliance
Aylena Hidalgo, MD
CRC / Pharmacist / Phlebotomy
Medical professional with international clinical training with clinical experience in Cuba and Angola and specialized experience in clinical research operations and infusion studies. Experienced in study coordination, informed consent, participant management, safety monitoring, infusion procedures, regulatory compliance, and clinical trial execution across multiple therapeutic areas.
Areas of Expertise
Clinical Trial Coordination | Infusion Study Management | Participant Recruitment & Retention | Informed Consent Process | Source Documentation & Data Quality | AE/SAE Identification & Reporting | Laboratory & Specimen Management | Regulatory Documentation Support | Vital Signs, EKGs & Safety Assessments | Investigational Product Coordination |Sponsor, CRO & Participant Communication | ICH-GCP & Research Compliance
Multilingual Patient Engagement: English, Spanish, Portuguese
Oriolma Martínez
CRC / Phlebotomy
Clinical research professional with experience in participant recruitment, informed consent, study coordination, participant safety monitoring, specimen collection, EKG performance, and clinical trial documentation. Experienced in supporting investigators and research teams while ensuring protocol compliance, participant safety, and high-quality data collection.
Areas of Expertise
Participant Recruitment & Screening | Informed Consent Process | Study Visit Coordination | EKG Performance | Vital Signs Collection | Participant Safety Monitoring | Clinical Documentation | Source Documentation | Laboratory Procedures & Specimen Handling | Adverse Event Reporting | Data Collection & Management | GCP Compliance