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(Senior) Bioanalytical Principal Investigator LBS / GLP Study Director (100%)
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Stellenbeschreibung
Overview In this role you lead regulated bioanalytical studies within the Ligand Binding Services group, acting as Study Director and PI to deliver compliant, high-quality data for global drug development. You will own study planning, validation, data review and client communication, shaping scientific outcomes and project success. The position offers exposure to innovative biologics and biomarkers in an international, science-driven CRO environment. You will mentor junior staff and contribute to business development and strategic client programs.
Leistungen / Benefits Flexible working hours Modern laboratories and state-of-the-art infrastructure Structured onboarding and professional development Attractive employment conditions Collaborative international environment Global career growth opportunities Verantwortungsbereiche Lead GLP/GxP-compliant bioanalytical studies and method validations in LBS Serve as Study Director and/or Principal Investigator with full study ownership Develop and approve study plans, validation protocols, analytical reports and study documentation Review and approve analytical data for scientific integrity and regulatory compliance Ensure activities comply with SOPs, regulatory requirements and client expectations Act as primary scientific/operational contact for assigned clients and provide updates Coordinate lab activities and ensure efficient study execution Train and mentor lab personnel and support
continuous quality improvements Support bioanalytical data management and documentation review For senior level: lead complex client programs, mentor juniors, act as SME in ligand-binding/cell-based assays, contribute to business development Zentrale Anforderungen Degree in Biochemistry, Biology, Chemistry or a related scientific discipline Minimum 2 years of experience in bioanalysis or quantitative analytical sciences Hands-on experience with ligand-binding assays and/or cell-based assays Experience in a regulated environment (GLP, GCP, GMP and/or ISO) Strong analytical thinking and problem-solving skills Excellent written and verbal English communication Ability to manage multiple projects with high quality and attention to detail Strong communication Project management Mentoring and leadership Ligand-binding assays Cell-based assays GLP/GxP compliance