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The Estée Lauder Companies attracts the most outstanding people from diverse industries and nurtures their talents. Whether they work in one of our stores, on a production line, at our corporate headquarters in New York City or in one of our affiliates worldwide, our employees take pride in their contributions to our success.

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The Estee Lauder Companies Clinical Senior Scientist in United States

Clinical Senior Scientist

Brand: Estée Lauder Companies


・ Manages day-to-day testing with external laboratories to ensure timely execution of clinical studies (sample registration and release, study protocol and report, data analytics and communication).

  • Create, manage, and archive documentation for clinical studies following GXP. Work with internal cross-functional partners to ensure data integrity and compliance.

  • Monitor/audit external laboratories to ensure fully compliance with internal and external requirement.

  • Performs other related duties as required by management which can include special projects or initiatives.

Reinforce ELC clinical capabilities in Asia. Perform clinical studies in Japan to support claims and formula development. Work closely with the Global Clinical team to coordinate the fielding of studies in Japan. Assure quality and data integrity in the execution of clinical studies. This position is primarily responsible for working with ELC approved clinical labs in Japan and coordinating the clinical testing for claims or innovation proof of concepts in accordance with Good Clinical Practices and company's SOPs. This position works closely with the Global Clinical team to field studies in Asia to fulfill claim support needs. This position's responsibilities review protocols, study report forms, informed consents and reports as needed; work the CRO to finalize study reports, perform data analysis, statistics.

Function as a clinical sponsor for studies performed at CROs in Japan. Assures that the protocols are accurate and fully supporting the established clinical plans with the appropriate parameters tested, timepoints included, methods applied, and studies performed in accordance with GCP and company's SOPs. Help develop the network of external partners, focusing on quality and data integrity. Assist the QA organization in auditing and monitoring clinical research organizations. Responsible for trial master files for clinical studies and R&D/Clinical database registration for the studies.

Stay current on trends in the cosmetic field, on clinical measurement science and technological developments and clinical methodology.

Respond to requests from management, as necessary


  • Must have experiences in clinical testing with 3 years in a clinical related role. Familiar with all the key clinical elements including recruiting, protocol, consent form, case report form, clinical measurement, study report and statistics.

  • Must have experiences working with external labs or CRO; experience in clinical testing in skincare preferred.

  • Experience with Good Clinical Practices and clinical study monitoring;

  • Ability to manage multiple projects in a fast-paced setting while maintaining attention to details and quality in the process..

  • Working knowledge of Microsoft Office applications: Word, Excel, and Outlook.

Job: Research & Development

Primary Location: Asia Pacific

Job Type: Standard

Schedule: Full-time

Shift: 1st (Day) Shift

Job Number: 200172

We are an equal opportunity employer. Minorities, women, veterans, and individuals with disabilities are encouraged to apply. It is Company's policy not to discriminate against any employee or applicant for employment on the basis of race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances. The Company will endeavor to provide a reasonable accommodation consistent with the law to otherwise qualified employees and prospective employees with a disability and to employees and prospective employees with needs related to their religious observance or practices. Should you wish to apply for this position or any other position with the Company and you believe you require assistance to complete an application or participate in an interview, please contact