Senior Scientist - In Vivo Pharmacology
Listed on 2026-10-28
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Research/Development
Research Scientist, Pharmaceutical Science/ Research
Medicilon USA Corp. is seeking an experienced Senior Scientist, In Vivo Pharmacology to lead and execute preclinical in vivo pharmacology studies supporting drug discovery and development programs. This role will be responsible for study design, execution, data interpretation, client communication, and development of new in vivo models and capabilities.
The ideal candidate has strong hands‑on experience with animal models, particularly oncology and emerging therapeutic modalities, and is comfortable working in a fast‑paced CRO environment where scientific quality, timelines, and client communication are equally important. The Senior Scientist will also mentor junior scientists and collaborate closely with Business Development, scientific teams, and Medicilon colleagues in China.
Key Responsibilities In Vivo Study Leadership & Execution- Lead in vivo efficacy and DMPK studies from study design through execution, data analysis, interpretation, and final reporting.
- Design study protocols and oversee study conduct, including cell culture, tumor cell inoculation, tumor measurement, dosing, sample collection, and other in vivo procedures as applicable.
- Analyze and interpret study data and clearly communicate results and scientific conclusions to internal teams and clients.
- Manage multiple studies and priorities while maintaining scientific quality and meeting aggressive project timelines.
- Maintain accurate, timely, and comprehensive study documentation in the electronic laboratory notebook (ELN) and other required systems.
- Serve as a scientific point of contact for assigned projects, providing timely study updates and responding to client questions.
- Work closely with project management and scientific teams to identify study risks, troubleshoot technical issues, and ensure successful project delivery.
- Participate in client meetings and scientific discussions as needed, including study planning, data review, and presentation of results.
- Independently design, develop, optimize, and validate new in vivo models based on client needs, market demand, and Business Development requirements.
- Conduct literature reviews and scientific assessments to evaluate new disease models, technologies, and experimental approaches.
- Support the development and validation of models for emerging therapeutic modalities, including biologics, CAR-T, gene therapy, and cell therapy.
- Contribute to expansion of Medicilon USA's in vivo pharmacology service platforms and scientific capabilities.
- Support in vitro and ex vivo studies when needed to complement in vivo programs.
- Support technical transfer, implementation, and validation of protocols and models from Medicilon's Shanghai scientific teams to the US laboratory.
- Collaborate with Business Development and Marketing teams to provide scientific expertise for client discussions, proposals, presentations, and other commercial activities.
- Work cross-functionally with scientists and operational teams in both the US and China to support project execution and capability development.
- Provide scientific guidance, training, and mentorship to junior research scientists and research associates.
- Support development of team capabilities, experimental standards, and scientific best practices.
- Foster a collaborative, accountable, and solutions-oriented laboratory environment.
- Perform all activities in accordance with applicable regulations, animal welfare requirements, Medicilon USA Corp. policies, SOPs, and quality standards.
- Ensure timely and accurate documentation of study activities and completion of all required training.
- Maintain high…
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