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Description

The Global Clinical and Consumer Science (GCCS) Department within R&D is engaged in conducting clinical / consumer studies at the Melville facility for evaluation of benefits of ELC’s skincare and makeup products and supporting competitive claims. This position serves a key role in assisting R&D scientists in the daily execution of human clinical studies. As a hands-on role in a laboratory setting, the position offers exposure to diverse study methods, cutting-edge instrumentation and an opportunity to interact with a diverse population of human panelists while working within a collaborative team.

Qualifications

Full time on-site role with direct engagement in skincare and makeup product testing to support claims, working within a dynamic team environment.

+ Associate Degree in Science or related field

+ 0-1 Years Experience

Must-Have Core Competencies:

+ Strong interpersonal and communication skills to collaborate effectively within a team and while interfacing with external participants in human clinical studies

+ Ability to operate under fast timelines and dynamic conditions

+ Proficient organizational and time management skills to manage multiple projects in a fast-paced setting

+ Demonstrate meticulous attention to detail to ensure accuracy and precision in testing techniques without compromising quality or compliance

+ Competent to prepare clear, accurate documentation in compliance with GxP and ALCOA+ principles

+ Ability to support extended day studies (11- 8 pm)

Preferred Qualifications:

+ Exposure to clinical environment or aesthetic dermatology

+ Familiarity with GCP / GxP

Essential operational functions include:

+ Execute study-related activities under supervision of the Scientist (informed consent, eligibility verification, imaging, instrumental measurements)

+ Prepare and review study documentation

+ Calibrate and maintain instruments

+ Order and re-stock lab supplies

+ Provide operational support for extended or evening clinical studies to validate long-wearing performance claims

+ Collect data on human subjects and maintain detailed documentation in accordance with Good Clinical Practices, data integrity principles, and company's SOPs

+ Perform post-study tasks, such as organizing documents, binder compilation, and review for accuracy and completeness

+ Monitor and identify panelist-related concerns, such as adverse product reactions or compliance issues, and promptly escalate these matters to the Supervisor to ensure the integrity and accuracy of clinical testing outcomes

+ Troubleshoot and escalate instrumentation issues as needed

+ Ensure all training including SOPs, GCP, GxP, is completed as per training schedule

Equal Opportunity Employer

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 [email protected].