NUVISAN The Science CRO
Pearle Ligeon has extensive work experience in the field of business development and management, with a focus on clinical research and quality assurance. Pearle is currently serving as the Director of Business Development at NUVISAN The Science CRO. Prior to this, they held the position of Associate Director of Business Development at CATO SMS. Pearle also worked as a Business Development Manager for Clinical Research Benelux at Sgs Belgium Nv. Pearle has a background in account management, having worked as an Accountmanager at Roche Diagnostics Nederland. Additionally, they have experience as a Certificate Lead Auditor at SGS and as a Clinical Research Associate at Quintiles. Pearle started their career as a Sales Executive at UCB. Pearle's work experience spans over two decades, with a range of responsibilities and expertise in various aspects of the industry.
Pearle Ligeon has pursued a Master's degree in Health Sciences from Maastricht University. Additionally, Pearle has also obtained a Bachelor's degree in Technical Sales Business from NCOI Opleidingen. However, specific details regarding the start and end years for both degrees are not provided.
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NUVISAN The Science CRO
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Founded in Europe with more than 40 years of experience, NUVISAN is a fully integrated contract research and development, and manufacturing organization (CRO/CDMO) that offers unique, high-quality, and tailored integrated solutions along the drug discovery and development value chain. With more than 1.000 employees distributed over six locations in Germany and France including our drug discovery hub in Berlin as well as with local experts situated in Latin America, NUVISAN is pleased to offer the following portfolio of services: • Drug discovery & research - Discovery pharmacology - Discovery bioscience - Screening - Life science chemistry - Translation research - Digital life science - Toxicology - DMPK • Non-clinical studies • Pharmaceutical analysis • Topical formulation development • Chemical development with GMP manufacturing (3-10kg) • Bioanalytical labs • GMP manufacturing (up to 50Kg) • Clinical trial supplies • Phase 1 and 2 clinical studies and beyond Our services can be provided as stand-alone or integrated solutions and can be customized to your project. Email us at hello@nuvisan.com for more.