Represent PK Sciences on a functional or cross-functional project team, or other science or business/operations team. Analyze data generated during any phase of project and present results with interpretation in a clear and concise manner.

Key responsibilities:

•Under guidance, represents PK Sciences as a sub-team member on project teams.

•Under guidance, write and contribute to transition documents (eg, DC and PPA) , clinical study protocols, clinical study reports, contribute to investigator brochures, IND / IMPDs and NDAs within agreed timelines, and meeting all regulatory requirements.

•Participates in, or under guidance leads PKS sub-team to generate, analyze, integrate data and identify project hurdles and mitigation for compound progression and development.

•Aligns plans and strategies with sub-teams, project teams, and leadership.

•May participate in cross-departmental teams, department-wide initiatives.

•Completes all required organizational trainings and requirements according to corporate timelines. Adhere in strict accord to the appropriate SOP

Essential requirements：

•0-2+ years in the pharmaceutical industry

•Relevant experience in drug metabolism, pharmacokinetics, clinical pharmacology, quantitative sciences, related research area. Appropriate training may be given.

•Knowledge of related disciplines (e.g., biostatistics, toxicology, regulatory) in the drug discovery or development process.

•Ability to work as part of a cross functional team in a highly dynamic, matrixed, project-team environment.

•Strong organizational and project skills with critical thinking and problem solving skills.

•Strong oral and written communication skills.

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