Job Summary:

InnoCare Pharmaceutical is seeking an exceptional PMO (Chief of Staff) to closely collaborate with and support the CEO in daily operations. The successful candidate will be responsible for executing initiatives from the CEO, as well as coordinating and managing key projects within the company.

Key Responsibilities:

1.Be responsible for elaboration of clinical development program strategy and planning, drive and guide the implementation of clinical development strategy, manage and control all the phases of clinical trials with all dimensions by establishing integrated, cross-functional, short-term and long-term program plans.

2.Serve as key contact for Clinical Development Program and related information, establish and maintain appropriate communications channels within and outside the Clinical Development Program Core Team, ensure sufficient and timely flow of information and communication, promote the identification and solution of problems., reporting directly to the CEO.

3.Engage in in-depth conversations with the CEO and the N-1 Top Management, documenting and organizing strategies for consensus and implementation.

4.Conduct or contribute to periodic key program review meetings (including, but not limited to Program Strategy meetings, Program Risk Management meetings, Lessons Learned or Program Budget reviews) in order to strive for earlier identification of critical success factors and to facilitate portfolio analysis, risk-management and decision-making; prepare meeting agendas and minutes and communicate action logs to improve the efficiency of core team.

5.Establish the implementation and tracking plans for project timeline and budget; accountable for ensuring the implementation of program/projects budget and progress; be responsible of optimized budget scenarios, maintain interaction partnership with key functions; propose the optimal clinical operations solutions and promote and maximize team work value through the integration and optimization of clinical development resource allocation.

Requirements:

1.Scientific Depth: Master in relevant scientific and/or medical, pharmacy, biology from a top university is preferred.

2.Rich experience in operation mode, workflow, ICH-GCP and other relevant regulations;

3.Rich experience in global clinical operation mode;

4.5+ years of relevant industry experience and 3+ year experience of global project management preferred;

5.Mature in conduct and demeanor, capable of handling external communications in significant situations.

6.Proficiency in English communication is required.