工作职责:
Key Responsibilities :
Typology Studies and in-house clinical studies
- Collaborates with key stakeholders to plan and execute typology studies/in-house clinical studies.
- Plans and designs research methods to achieve project objectives/deliverables/milestones.
- Ensure studies adhere to Chinese regulations and standard, e.g. IRB application
- Analyses and interprets data to make conclusions/recommendations for product concept
- Prepares and presents reports to key stakeholders.
- Scientific monitoring (competitor's publications and new findings)
External claim study
- Collaborates with agency to plan and execute claim studies.
- Prepares reports/clinical briefs to key stakeholders.
Organizational Excellence
- Supports workforce planning, enhance staff knowledge and expertise over time.
- Trains technicians and interns
- Cultivates and maintains strong collaborative relationships with internal and external partners
Project Management
- Plans and develops project proposals and executes project objectives in line with Clarins guidelines and best practices.
- Ensures processes and protocols compliance: all studies (in-house or external) should comply with Chinese regulations/guidelines and Clarins laboratories SOP/guidelines.
- Tracks, monitors, reviews, manages, and reports studies progress. Ensure all milestones are met.
- Uses knowledge of statistics and experimental design to support project planning and data interpretation and reporting.
- Responsible for the health, safety, hygiene, ethical, and financial integrity of all projects undertaken.
Member Of a Project Team
- Undertakes designated tasks as a responsible member of the R&D team.
- In association with other researchers in the team, be a source of clinical evaluation expert for colleagues and stakeholders
- Recognises the need and desire to undertake personal development as the role develops
任职条件:
- Bachelor or Master of Science in Chemical/Biology.
- Minimum of 3-5 years Clinical evaluation experience, with broad knowledge base and understanding.
- Demonstrated ability to develop, undertake and manage intervention projects.
- 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.
- Understands and interprets relevant rules and regulations, adherence to ethical practices in human research studies, and Chinese regulations.
- 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.
- Strong communication skills, both written and oral in both English and Chinese, to effectively promote and present results to key stakeholders.
- Team-oriented, collaborative, and capable of working in a global company and with diverse cultures.
- 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.
- Available for domestic and international travel (~10%).