Orum Therapeutics

Human Resources

• Support day-to-day HR operations including payroll coordination via external vendors as needed
• Contribute to operational accuracy and process stability in a lean team environment
• Collaborate with Finance and IR to provide accurate HR data for corporate disclosures and ensure compliance with KOSDAQ requirements
• Support tax-related processes for equity programs, including withholding tax handling and coordination with relevant stakeholders and external vendors
• Assist with compliance-related documentation and reporting for public company requirements
• Evaluate and improve current stock-based compensation programs (Stock Options, etc.)
• Support the design and implementation of new equity incentive schemes aligned with a KOSDAQ-listed environment and global growth
• Support operational processes related to stock option exercises, taxation, and equity administration
• Conduct data-driven compensation benchmarking and analyze peer group data within the industry to support informed salary and incentive decisions
• Refine, administer, and continuously improve existing Total Rewards programs integrating cash, benefits, and equity to support high talent density and long-term retention
• Work with the global HR team to develop and improve internal HR workflows, documentation, and employee-facing materials (e.g., onboarding guides, welcome handbooks) to enhance operational efficiency and employee experience
• Participate in and support key HR initiatives, including the introduction of new equity programs and the setup of HR processes for new international entities
• Support implementation and operationalization of evolving global reward programs
• Support HR forecasting and operational follow-up processes, including workforce planning, compensation tracking, and coordination of ongoing HR initiatives

HR Manager

Research Scientist

• Design, oversee, and interpret IND-enabling nonclinical toxicology studies for DAC programs.
• Serve as the nonclinical toxicology lead on assigned DAC programs, providing scientific input on nonclinical safety assessment, risk identification, and mitigation strategies.
• Support clinical starting dose selection and risk assessment in collaboration with DMPK and clinical development teams.
• Author and contribute to nonclinical sections of INDs and related regulatory documents.
• Collaborate close with pharmacology, DMPK, pathology, bioanalytical, CMC, regulatory affairs, and clinical development teams.
• Manage external CROs and consultants, ensuring scientific quality, timelines, and budget adherence.

HR Manager

Senior Principal Scientist – Toxicology