KEY ACCOUNTABILITIES

？ Lead clinical pharmacology outsourcing to support China projects

o Maintai a robust and effective relatiohip with preferred partner CROs in given projects and manages any issues to an effective resolution.

o Eure development and delivery of clinical bioanalytical strategy.

o Be respoible for quality aspects by supporting in- and external audit/ipection.

？ Contribute scientific excellence to China projects

o Represent GED/Clinical Pharmacology in China Program/Project Teams.

o Contribute to clinical protocol design, operation planningampling logistics.

o Participate in clinical report and regulatory dossier preparatioreview.

？ Involve in China and pan-Asian R&D strategic discussion

o Seek opportunity for innovative early development pathways.

o Bring integrated thinking and planning cross disciplines with other China R&D line functio.

o Engage in joint China-Japan strategic planning.

EDUCATION

？ PhD or Master’s degree in pharmaceutical, biological or related field with 3-5+ yea of post-graduate

？ experience in the life sciences industry.

？ Excellent verbal and written communication skills in English.

WORK EXPERIENCE

？ Experience working with a CRO or external partner.

？ Good undetanding of drug discovery and development process, preferably with working experience in GLP and/or GCP.

？ Prior project management, project coordination, and/or contract and budget management experience.

？ General undetanding of pharmacokinetics, pharmacodynamics, and biomarke.

？ Familiar with regulatio and guidelines from regional health authorities (e.g. CFDA).

？ Experience working in global setting with multi-cultural awareness.