Orum Therapeutics

Conversion Rate Optimizer

• Oversee the external development of our Degrader-Antibody Conjugate (DAC) pipeline
• Manage high-stakes projects at CROs, specifically overseeing the synthesis of proprietary molecular glue degrader payloads and their conjugation to therapeutic antibodies
• Proactively identify and vet CROs that offer specialized expertise in relevant in-vitro activity assays, in vivo studies, linker-payload synthesis, and complex bioconjugation
• Support the expansion of our TPD²® (Degradation) and TPS²™ (Stabilization) platforms by identifying specialized Chinese partners capable of advanced physics-based modeling and machine learning-driven payload design
• Drive IND-enabling studies for candidates like ORM-1153 (CD123-targeting DAC) and support ongoing clinical-stage programs
• Navigate the "China price" ecosystem to find cost-effective, high-quality alternatives for R&D without compromising the integrity of our AnDC™ (Antibody neoDegrader Conjugate) technology

External Research Leader – CRO

Manager

• 공시 사업보고서, 분·반기보고서, 주요사항보고 등 정기·수시 공시 작성 및 제출
• 다양한 공시 사이클(정기/비정기/이슈성) 운영 및 관리
• KOSDAQ 공시 규정 준수 및 KRX·FSS 대응
• 공시 일정 및 프로세스 관리
• 전환사채, 증자 등 자본시장 관련 공시 업무 지원
• 외부 감사인 및 법무 자문과 협업하여 정기 보고서 기재 내용 관리
• IR 및 대외 커뮤니케이션(필요 시)
• IR 자료 및 공시 연계 자료 작성·업데이트
• 실적 발표, 투자자 미팅 등 IR 활동 지원
• 공시 내용과 대외 메시지 간 일관성 확보
• 주식기반보상(Equity Compensation) 주식기반보상 관련 공시 및 내부 절차 운영
• 주식기반보상 행사·베스팅 등과 관련된 행정 및 유관 부서 협업
• 주식기반보상 관련 이사회·주주총회 안건 지원

Disclosure Manager, IR

Research Scientist

• Design, oversee, and interpret IND-enabling nonclinical toxicology studies for DAC programs, including GLP toxicology, safety pharmacology, and toxicokinetic assessments.
• 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 closely with pharmacology, DMPK, pathology, bioanalytical, CMC, regulatory affairs, and clinical development teams.
• Manage external CROs and consultants, ensuring scientific quality, timelines, and budget adherence.

External Research Leader – CRO

Disclosure Manager, IR

Senior Principal Scientist – Associate Director, Toxicology