Medicilon USA Corp is seeking a Senior Scientist with strong expertise in in vitro and in vivo pharmacology to lead study execution, scientific strategy, and client-facing activities. This role plays a key part in delivering high-quality preclinical studies and expanding our pharmacology platforms.
The ideal candidate brings hands-on experience in assay development and animal models, thrives in a fast-paced CRO setting, and can bridge scientific execution with client needs.
Key Responsibilities
Scientific Leadership & Study Execution
- Design and lead in vitro and in vivo pharmacology studies, including protocol development, execution, data analysis, and reporting.
- Develop, optimize, and validate assays such as cell-based assays, efficacy models, PK/PD-related studies, and biomarker analysis.
- Oversee study conduct to ensure scientific rigor, reproducibility, and alignment with client objectives.
- Interpret data and generate clear, decision-ready insights for internal teams and clients.
- Evaluate new techniques and models to expand pharmacology capabilities.
Project & Client Management
- Serve as a scientific lead on client projects, participating in study design discussions, troubleshooting, and results presentation.
- Work closely with Project Managers and cross-functional teams to ensure timelines and deliverables are met.
- Prepare reports and presentations for both technical and non-technical audiences.
- Maintain accurate and compliant documentation using ELN systems.
Quality & Operational Excellence
- Support GLP-like practices and QMS, including SOP development and adherence to audit-ready standards.
- Assist in technology transfer and platform setup (including collaboration with China teams where applicable).
- Contribute to continuous improvement of workflows, assay robustness, and data quality.
Team Leadership & Mentorship
- Mentor and guide junior scientists and research associates in experimental design and execution.
- Support onboarding and training to build team capability and consistency.
Business Support
- Partner with Business Development by providing scientific input for proposals, capabilities discussions, and client engagement.
Qualifications
- Ph.D. in Pharmacology, Biology, Immunology, or related field with 5+ years of industry/CRO experience.
- Strong hands-on experience in in vitro assays and in vivo pharmacology models.
- Proven ability to lead studies end-to-end and manage multiple projects.
- Familiarity with GLP/QMS standards and working in a client-driven environment.
- Strong communication skills, with the ability to present data clearly to clients.
- Experience mentoring or supervising junior staff preferred.
- Prior client-facing or CRO experience strongly preferred.