Jocelyn Morera is a Clinical Research Coordinator at NewGen Health Group with extensive experience supporting Phase I-IV clinical trials across vaccines, infectious diseases, neuroscience, psychiatry, pulmonology, cardiometabolic disorders, and other complex therapeutic areas. She plays an integral role in study execution, participant management, laboratory operations, and data quality oversight, helping ensure successful clinical trial outcomes. 

Ms. Morera has contributed to numerous studies sponsored by leading pharmaceutical companies, including Pfizer, Moderna, Bristol Myers Squibb, Janssen, Sanofi, and GlaxoSmithKline. Her experience includes vaccine development programs, Alzheimer’s disease, major depressive disorder, COPD, heart failure, obesity, infectious diseases, and other innovative clinical research initiatives. 

She is highly skilled in patient recruitment, informed consent, study coordination, source documentation, specimen collection and processing, data management, and protocol compliance. Her certifications in Good Clinical Practice (GCP), phlebotomy, bloodborne pathogens, OSHA compliance, and clinical research operations reflect her commitment to maintaining the highest standards of patient safety and data integrity. 

As part of the NewGen Health Group team, Ms. Morera is dedicated to delivering exceptional participant experiences while supporting sponsors with accurate data collection, protocol adherence, and operational excellence. Her attention to detail, strong organizational skills, and patient-centered approach make her a valuable asset in the successful execution of clinical trials. 

• Experienced Clinical Research Coordinator supporting Phase I-IV studies.
• Extensive vaccine and infectious disease research experience.
• Strong patient recruitment, enrollment, and retention capabilities.
• Skilled in laboratory procedures, specimen processing, and phlebotomy. 
• Experienced in source documentation, EDC systems, and data management.
• Certified in GCP, phlebotomy, bloodborne pathogens, and clinical research compliance.
• Experience supporting studies across neurology, psychiatry, pulmonology, cardiology, obesity, and vaccine development.
• Dedicated to participant safety, protocol compliance, and high-quality data collection.
• Strong focus on operational excellence and sponsor satisfaction.