Hartmann Young · 5 hours ago
Senior Clinical Scientist
Hartmann Young is seeking a Senior Clinical Scientist to support the advancement of a first‑in‑class targeted biologic therapy for hematologic malignancies. This role involves early clinical strategy, trial design, and data interpretation within a lean, science‑driven biotech environment.
Responsibilities
Support first‑in‑human and Phase 1/1b clinical studies in hematologic malignancies
Contribute to development of dose‑escalation strategies, safety monitoring plans, and clinical endpoints appropriate for early signal detection
Participate in ongoing safety and data review, including dose‑escalation and internal governance discussions
Translate preclinical and translational datasets into clear clinical hypotheses and development decisions
Support dose selection rationale, pharmacokinetic and pharmacodynamic assessments, and biomarker integration
Collaborate closely with translational and discovery colleagues to ensure alignment between mechanism of action and clinical readouts
Contribute to clinical protocols, investigator brochures, and study‑level documents
Support preparation of materials for regulatory interactions, including briefing documents and responses
Participate in IND‑maintenance activities as the program transitions into clinical execution
Work closely with Clinical Operations, Biostatistics, Safety, Regulatory, and Translational teams
Provide scientific guidance to CRO partners and study teams to ensure high‑quality study conduct
Support investigator engagement, including scientific discussions and investigator meetings
Qualification
Required
Advanced scientific degree (PhD, PharmD, MD, or MSc with relevant experience)
5+ years of experience in clinical development within biotech or pharma
Demonstrated experience supporting early‑phase oncology or hematology clinical trials
Strong understanding of hematologic malignancies, particularly myeloid or molecularly defined diseases
Experience working on biologic therapies (e.g. monoclonal or engineered antibodies)
Hands‑on experience with clinical data review and interpretation
Familiarity with IND‑stage development and first‑in‑human regulatory expectations
Excellent communication skills and ability to work effectively in cross‑functional teams
Preferred
Direct experience supporting first‑in‑class or mechanism‑driven programs
Exposure to small, genetically or molecularly defined patient populations
Experience contributing to regulatory agency interactions
Prior experience in an early‑stage or growth‑stage biotech
Company
Hartmann Young
Hartmann Young offers executive staffing for life sciences, focusing on talent connections in the Asia Pacific region.
Funding
Current Stage
Early StageRecent News
2025-11-04
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