Joselin Hernandez, CRC

Joselin Hernandez, CRC

Study Coordinator

Experience: 4 years
Role: Study Coordinator
Languages: English / Spanish

Core Strengths

Study 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.

Experience

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.

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.

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