(Senior) Bioanalytical Principal Investigator LBS / GLP Study Director (100%)

Responsibilities

• Lead and oversee GLP/GxP-compliant bioanalytical studies and method validations within the Ligand Binding Services (LBS) department.
• Act as Study Director and/or Principal Investigator with full responsibility for assigned studies or study phases.
• Develop and approve study plans, validation protocols, analytical reports and associated study documentation.
• Review, evaluate and approve analytical data to ensure scientific integrity and regulatory compliance.
• Ensure all study activities are conducted in accordance with applicable SOPs, regulatory requirements and client expectations.
• Serve as the primary scientific and operational contact for assigned clients.
• Provide regular project updates and maintain strong communication throughout the study lifecycle.
• Support client meetings, scientific discussions and audits as required.
• Coordinate laboratory activities and ensure efficient study execution.
• Train, mentor and support assigned laboratory personnel.
• Contribute to process improvements and continuous enhancement of laboratory operations and quality standards.
• Support bioanalytical data management activities and documentation review processes.

Requirements

• Degree in Biochemistry, Biology, Chemistry or a related scientific discipline; PhD is advantageous.
• Minimum 2 years of experience in bioanalysis or quantitative analytical sciences.
• Hands-on experience with ligand-binding assays and/or cell-based assays.
• Experience working in a regulated environment (GLP, GCP, GMP and/or ISO standards).
• Strong analytical thinking and problem-solving skills.
• Excellent written and verbal communication skills in English.
• Ability to manage multiple projects while maintaining a high level of quality and attention to detail.

Nice to have

• Previous experience as a Study Director, Principal Investigator or equivalent scientific leadership role.
• Knowledge of biomarker, pharmacokinetic (PK), immunogenicity (ADA) or biologics bioanalysis.
• Good German language skills.
• Experience working directly with pharmaceutical or biotechnology clients.

What the company offers

• The opportunity to lead scientifically challenging projects for global pharmaceutical and biotech clients.
• Exposure to innovative biologics, biomarkers and emerging therapeutic modalities.
• A collaborative, international and science-driven working environment.
• Structured onboarding and continuous professional development opportunities.
• Modern laboratories and state-of-the-art infrastructure.
• Flexible working hours and attractive employment conditions.
• The opportunity to grow your career within a globally recognized CRO.
• A workplace located near Zurich with easy access to excellent public transportation and recreational opportunities.