A dedicated biomedical scientist with specialized expertise in genetics, grounded in biomedical sciences and cell biology, and interested in transitioning into the pharmaceutical and biotech sectors. Skilled in conducting in-depth research on genetic diseases, contributing to advancements in diagnostics, treatments, and patient care. Experienced in both statistical and qualitative analysis of complex data sets, applying cutting-edge techniques to uncover genetic insights in rare diseases. Possesses a comprehensive understanding of molecular mechanisms and extensive hands-on experience in laboratory techniques, enabling valuable contributions to research teams and driving scientific outcomes. Fluent in German, facilitating collaboration across multinational environments and diverse research settings, with a strong commitment to leveraging expertise for impactful advancements in public health .
· Builds and maintains collaborative relationships with 4 out of 15 statewide metabolic and genetic teams, enhancing communication and improving care coordination for newborns, including managing follow-up care for 989 babies diagnosed with rare genetic conditions.
· Oversees confirmed cases of four rare genetic diseases, including Spinal Muscular Atrophy (SMA), Pompe disease, Mucopolysaccharidosis type I (MPS-1), and Biotinidase deficiency, ensuring adherence to clinical best practices and regulatory standards.
· Achieves a 95% compliance rate with regulatory requirements by closely monitoring adherence and addressing deviations through proactive measures.
· Improves program efficiency by consistently monitoring and assessing project progress, leading to a 20% reduction in follow-up times and faster intervention.
Develops and delivers customized educational materials for over 500 patients, addressing diverse levels of health literacy and ensuring better understanding of complex genetic information
· Contributed to the development of clinical study policies and programs, emphasizing human subject protection, and provided analytical insights that influenced key decisions in over 20 medical device evaluations.
· Led and coordinated clinical trials from inception through completion, achieving an average patient retention rate of 95%.
· Designed and developed study protocols, case report forms (CRFs), and informed consent documents for over 30 clinical trials, ensuring adherence to trial objectives and compliance requirements.
· Managed patient recruitment and enrollment, successfully enrolling over 100 participants across multiple trials, while maintaining comprehensive and accurate patient records, including informed consent documentation.
· Coordinated all logistical aspects of clinical trials, scheduling over 500 patient visits and overseeing lab work, imaging studies, and investigational drug administration.
· Monitored patient responses and adverse events, ensuring 100% timely reporting to study teams and regulatory authorities, while maintaining meticulous study documentation for over 2,000 case report forms in compliance with Good Clinical Practice (GCP) standards.
Dr. Deidre Devier, ddevie@lsuhsc.edu
Full-time