Laboratory Technician

Randstad Enterprise; Melville (NY); On-site; USD 31,000 - 44,000; Full time

Job summary

Randstad Enterprise in Melville, NY is seeking a Laboratory Technician- Clinical Testing for a 6-month W2 contract. This on-site role supports clinical studies in skincare, with exposure to instrumentation and human panelists.

Hours are Mon-Fri 7:00 am-3:30 pm with a 30 min lunch; extended studies may require 11 am-8 pm. Pay is $27 per hour. The position emphasizes GxP compliance, precise documentation, and collaboration with R&D scientists.

Qualifications

• Strong interpersonal and communication skills for team collaboration and participant interfacing.
• Ability to operate under fast timelines and dynamic conditions.
• Proficient organizational and time-management skills for multiple projects.
• Meticulous attention to detail to ensure testing accuracy and compliance.
• Prepare clear documentation in line with GxP and ALCOA+.

Responsibilities

• Execute study-related activities under supervision (consent, eligibility verification, imaging, measurements).
• Prepare and review study documentation.
• Calibrate and maintain instruments.
• Order and re-stock lab supplies.
• Provide operational support for extended or evening studies (11am–8pm).
• Collect data on human subjects and document per SOPs.
• Post-study tasks: organize documents and ensure accuracy.
• Monitor panelist concerns and escalate to maintain testing integrity.
• Troubleshoot instrumentation issues as needed.
• Ensure training on SOPs, GCP, and GxP is completed.

Skills

Interpersonal skills

Communication

Time management

Attention to detail

GxP documentation

ALCOA+ principles

Extended-day support

Job description

Job title: Laboratory Technician- Clinical Testing

End date: 6/14/27 (6 Month Contract Duration- W2)

Hours: Monday-Friday 7:00am-3:30pm with 30 minute unpaid lunch break totaling 40 hours per week. Candidates may need to flex their schedule for extended studies testing completed 2-6x per month. The hours during the extended studies is 11am-8pm.

Location: Fully on-site at 155 Pinelawn Road Melville, NY

Pay Rate: $27.00 per hour

The Global Clinical and Consumer Science (GCCS) Department within R&D is engaged in conducting clinical / consumer studies for evaluation of benefits of skincare and makeup products to support 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.

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.
• Adept to prepare clear, accurate documentation in compliance with GxP and ALCOA+ principles.
• Ability to support extended day studies (11am- 8 pm).

Preferred Qualifications:

• Makeup artistry.
• Exposure to clinical environment or aesthetic dermatology.

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 the Supervisor to ensure the integrity and accuracy of clinical testing outcomes.
• Troubleshoot and elevate instrumentation issues as needed.
• Ensure all training, including SOPs, GCP, GxP, is completed as per training schedule.