Most recently Renee C. St.Clair, Esq. was In-House Counsel for Valis Biosciences Inc, where she also served at the Regulatory Affairs, Operations, and Compliance Lead. Ms. St.Clair has over 25 years of legal and regulatory experience advising California employers, is the co-founder of a woman owned law firm based in San Diego, California, and is a specialist in appellate research and writing, including a successful appeal to the U.S. Supreme Court.
Ms. St.Clair pivoted to the life sciences industry hoping to apply her legal skillset to advance science, medicine, and patient outcomes; particularly for patients and veterans struggling with mental health issues. She has a unique perspective, having been on various sides of the clinical trial process. Ms. St.Clair provided regulatory guidance at one of the first clinical trial sites in the world to administer psilocybin to participants with depression, has worked with R&D scientists as they developed clinical trial protocols for ketamine, co-drafted IND applications, transitioned a biopharma lab from R&D to GMP-readiness, positioned a biopharma company to obtain state authorization to conduct nonhuman research of Schedule I compounds (DMT, LSD, psilocin, THC, MDMA, 5-MEO-DMT), and currently applies her regulatory background to facilitate Valis Biosciences Inc.’s science based and technology driven clinical trial tools and solutions—often in challenging populations (children) or difficult to measure conditions (mental health and CNS).
Michael Gülck has been with Chevron since January 2015. As a Business Development Specialist Michael is responsible for the development of Chevron’s premium gas engine products (HDAX and coolant DELO XLC) in Europe, Africa and Russia.
Michael has been working in the global CHP industry for over 37 years. In this time, he has acquired key knowledge and insight from successful CHP manufacturers across the globe, including Jenbacher and Caterpillar.
Michael has provided international training courses, lectures, and webinars over the last 25 years. Whether electrical integration, hydraulic problems, CHP management, damage analysis or CHP economic considerations, Michael is always available to advise his customers and partners on solutions.
As a seasoned global leader, I’ve delivered concrete business outcomes and enhanced productivity. My unwavering dedication to customer satisfaction and team growth has been instrumental in propelling organizational success. Proficient in navigating intricate transformations, I’ve elevated staff engagement and strategically harnessed existing technologies for a competitive edge. Aligning operational strategies with company goals, I’ve successfully executed significant projects across diverse contexts. My strength lies in fostering collaboration, establishing partnerships at all organizational levels, and implementing practical business solutions across cultural landscapes. My unwavering commitment to operational excellence has streamlined manufacturing and logistics facilities, enhancing efficiency. Throughout my career, I’ve contributed to a prominent organization known for exceptional manufacturing and engineering capabilities in the life sciences sector
Experienced outsourcing professional with passion for clinical technology and clinical research in the oncology field.
A highly motivated, experienced IT Product Management professional with over 26 years of experience in the biopharmaceutical service industry. Executes product strategy, defines product vision and roadmaps, develops customer-driven product requirements incorporating human-centered design, drives product release cycles using Agile methodologies, and collaborates with cross-functional teams to deliver high quality solutions on time. Prior roles include IT Product Owner, IT Business Partner, Integrated Processes and Technologies POC Project/Product Manager, Predictive Analytics Lead SAS Developer, Biostatistics Senior SAS Statistical Programmer, Statistical Programming Manager, Clinical Data Programmer, and Associate Biostatistician.
