Key Responsibilities:

Typology Studies and in-house clinical studies
1. Collaborates with key stakeholders to plan and execute typology studies/in-house clinical studies.
2. Plans and designs research methods to achieve project objectives/deliverables/milestones.
3. Ensure studies adhere to Chinese regulations and standard, e.g. IRB application
4. Analyses and interprets data to make conclusions/recommendations for product concept
5. Prepares and presents reports to key stakeholders.
6. Scientific monitoring (competitor’s publications and new findings)


External claim study
1. Collaborates with agency to plan and execute claim studies.
2. Prepares reports/clinical briefs to key stakeholders.


Organizational Excellence
1. Supports workforce planning, enhance staff knowledge and expertise over time.
2. Trains technicians and interns
3. Cultivates and maintains strong collaborative relationships with internal and external partners

Project Management
1. Plans and develops project proposals and executes project objectives in line with Clarins guidelines and best practices.
2. Ensures processes and protocols compliance: all studies (in-house or external) should comply with Chinese regulations/guidelines and Clarins laboratories SOP/guidelines.
3. Tracks, monitors, reviews, manages, and reports studies progress. Ensure all milestones are met.
4. Uses knowledge of statistics and experimental design to support project planning and data interpretation and reporting.
5. Responsible for the health, safety, hygiene, ethical, and financial integrity of all projects undertaken.

Member of a Project Team
1. Undertakes designated tasks as a responsible member of the R&D team.
2. In association with other researchers in the team, be a source of clinical evaluation expert for colleagues and stakeholders
3. Recognises the need and desire to undertake personal development as the role develops


Key Requisition:
1. Bachelor or Master of Science in Chemical/Biology.
2. Minimum of 2 years Clinical evaluation experience, with broad knowledge base and understanding.
3. Demonstrated ability to develop, undertake and manage intervention projects.
4. Sound knowledge and demonstrated experience in clinical evaluation, clinical briefs, statistical analysis, practices, and procedures that would be acquired through experience with cosmetic research studies, familiar with cosmetic in-vivo test especially.
5. Understands and interprets relevant rules and regulations, adherence to ethical practices in human research studies, and Chinese regulations.
6. Demonstrated capacity to build relationships with team members and to perform effectively in a team environment, to work closely with support staff and key stakeholders.
7. Strong communication skills, both written and oral in both English and Chinese, to effectively promote and present results to key stakeholders.
8. Team-oriented, collaborative, and capable of working in a global company and with diverse cultures.
9. High level of organizational, prioritization, and project management skills, problem-solving orientation, and desire to innovate in a fast-moving environment with sufficient sense of urgency to meet imposed timelines.
10. Available for domestic and international travel (~10%).

其他信息
语言要求：英语、普通话

所属部门：R&D