Study Coordinator

Adriana Crespo, CRCStudy Coordinator Experience: 4 years Role: Study Coordinator Languages: English / Spanish (786) 464-0732Core StrenghtsStudy Coordination 100%Documentation & Compliance 100%Sponsor & Site Communication 100% About Me As a Study Coordinator at Hope Clinical Trials, she supports the successful execution of clinical research studies from participant enrollment through study completion. Her role brings together patient coordination, protocol implementation, study documentation, and communication with investigators and research partners to help ensure trials are conducted efficiently and in accordance with study requirements. With CRC certification and hands on experience supporting clinical research operations, she serves as an important connection between study participants, investigators, sponsors, monitors, and the broader research team. Her organized and detail oriented approach helps maintain study continuity while supporting accurate documentation, timely follow up, and a positive participant experience. ExperienceRole in Clinical Research Clinical trials depend on careful coordination across many moving parts. As Study Coordinator, she helps manage day to day study activities, supports participant scheduling and follow up, assists with study documentation, and works with the clinical team to keep research activities aligned with protocol requirements and study timelines. She also helps facilitate communication with external research partners, providing the organization and responsiveness necessary to support productive sponsor and site relationships throughout the lifecycle of a study. Research Partner Focus Her approach to study coordination emphasizes preparedness, responsiveness, and attention to detail. She understands that successful research sites must balance the needs of participants with the operational and documentation requirements of sponsors and research partners. This makes her role particularly important in helping Hope Clinical Trials maintain organized study operations, respond efficiently to study needs, and support dependable execution across active protocols.

Lyanie Gonzalez, CRCStudy Coordinator Experience: 2 years Role: Study Coordinator Languages: English / Spanish (786) 464-0732Core StrengthsOrganization & Follow Through 100%Participant Coordination 100%Team Collaboration 100% About Me Lyanie Gonzalez is a Clinical Research Coordinator at Hope Clinical Trials, where she supports the day to day coordination and execution of clinical research studies. Working closely with investigators, study participants, and the broader research team, she helps ensure that study activities remain organized, timely, and aligned with protocol requirements. As a CRC, Lyanie assists with participant scheduling and follow up, study visit preparation, research documentation, and coordination of protocol related activities. She brings a detail oriented and collaborative approach to her work, helping create an efficient research environment while ensuring participants receive clear communication and consistent support throughout their involvement in a clinical trial. Lyanie is committed to continuing to expand her experience in clinical research while contributing to Hope Clinical Trials' mission of providing patients access to emerging treatment options through high quality, patient focused research. ExperienceRole in Clinical Research Lyanie supports the operational details that help clinical trials move successfully from enrollment through study completion. Her responsibilities include coordinating participant visits, assisting with study documentation, maintaining communication with participants, and working alongside investigators and other research professionals to support protocol execution. Approach to Study Coordination Lyanie approaches clinical research with an emphasis on organization, accuracy, communication, and follow through. She understands that even small operational details can have an important impact on participant experience and study quality, and she works to help keep each study organized and moving forward.

Joselin Hernandez, CRCStudy Coordinator Experience: 4 years Role: Study Coordinator Languages: English / Spanish (786) 464-0732Core StrengthsStudy Coordination 100%Participant Engagement 100%Multidisciplinary Collaboration 100% Biography Joselin Hernandez is a Clinical Research Coordinator with more than four years of experience supporting Phase II through Phase IV clinical trials across multiple therapeutic areas, including neurology, immunology, and infectious diseases. At Hope Clinical Trials, she helps coordinate study activities, participant visits, follow up, documentation, and communication across the research team to support efficient and well organized study execution. Her professional background includes certifications in Good Clinical Practice, Clinical Research Coordination, IATA, CPR, AED, and First Aid. She is fluent in English and Spanish and brings a strong commitment to patient advocacy, healthcare access, and culturally responsive communication. Joselin is known for her organization, adaptability, and collaborative approach. She works effectively across multidisciplinary teams and helps maintain the consistency, responsiveness, and attention to detail that are essential to high quality clinical research. ExperienceApproach to Clinical Research Joselin views strong study coordination as a balance between precise operational execution and meaningful participant support. She works to keep study activities organized, anticipate upcoming requirements, and maintain clear communication among participants, investigators, and research partners. Her developing clinical background in physical therapy also strengthens her appreciation for functional health, recovery, mobility, and the importance of evaluating outcomes that matter in everyday life. Role in Study Operations As a Study Coordinator, Joselin helps support participant scheduling, study visit preparation, research documentation, follow up activities, and communication with the broader clinical research team. Her role contributes to consistent study execution by helping ensure that required activities are completed according to protocol and within appropriate timelines. This coordination supports both participant retention and the operational reliability expected by sponsors and research partners.