Actively shape the cybersecurity and resilience of a global, highly regulated company as a Business Information Security Officer (BISO), acting as a central interface between Business, IT, and Operational Technology (OT).
Compensation
Nach österreichischem Recht sind wir verpflichtet, das kollektivvertragliche Mindestgehalt bekannt zu geben, das sich für diese Stelle auf EUR 79.951,48 / Jahr (auf Vollzeitbasis) beläuft.
Responsibilities
Manage NIS2 Technology Readiness Activities and conduct Cyber Risk Assessments (CRA) across Sandoz companies with production or development capacities
Monitor Cyber and Information Security Compliance in local Operational Technology (OT) environments
Act as a central interface to local and regional Sandoz Leadership Teams (SLTs)
Observe country- and region-specific cyber threats and regulatory developments (NIS2, GDPR)
Promote the harmonization of global cybersecurity services across countries and regions
Requirements
Completed degree in Computer Science, Electrical Engineering, Mathematics, or a related field
Responsible for providing data management services for clinical trials, ensuring on‑time and accurate deliverables, and supporting global clients across time zones.
Responsibilities
Provide data management guidance to internal project team members and customers
Communicate with internal project team members and customers on all aspects of data management activities
Author data management documents
Perform user acceptance testing on data management deliverables
Facilitate and verify data clarifications and data changes
Requirements
BA/BS degree in a relevant field (Medicine, Statistics, Computer Science) or equivalent work experience
Lead and manage GCP quality strategy and oversight across Denali’s clinical trial portfolio, ensuring compliance, risk management, and continuous improvement.
Compensation
Salary Range: $171,000.00 to $223,000.00 . Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience.
Responsibilities
Lead GCP quality strategy on assigned Study Execution Teams
Partner with Zurich Site Lead and cross-functional leaders to drive site-level quality maturity
Lead proactive quality risk assessments and drive risk mitigation strategies
Own risk-based monitoring and analysis of quality issues
The Director, Global PV Management is responsible for assessing regional and international pharmacovigilance regulatory requirements and translating them into effective drug safety & pharmacovigilance procedures and operational processes.
Locations (3)
San Francisco, California, United States
San Diego, California, United States
Princeton, New Jersey, United States
Compensation
$194,600—$243,300 USD
Responsibilities
Review and interpret applicable international and regional pharmacovigilance regulatory requirements
Continuously monitor changes to pharmacovigilance requirements in countries where the company operates
Assess pharmacovigilance requirements for new countries and develop operational readiness plans
Conduct and document gap assessments comparing regulatory requirements with existing SOPs
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