Clinical Laboratory Technician

Actalent Inc

  • Las Vegas, NV
  • 3 days ago
  • $21 Per Hour

Highlights

This role supports a clinical research unit by working closely with floor technicians and phlebotomists to collect, organize, and process pharmacokinetic (PK) samples in a small laboratory adjacent to the clinic floor. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

Numbers & Facts

LocationLas Vegas, NV

Description

Job Title: Clinical Laboratory Technician

Job Description

This role supports a clinical research unit by working closely with floor technicians and phlebotomists to collect, organize, and process pharmacokinetic (PK) samples in a small laboratory adjacent to the clinic floor. The clinical laboratory technician focuses on processing blood and urine specimens from healthy subjects participating in overnight Phase I studies, ensuring that all samples are collected and handled according to study protocols and regulatory standards. The position contributes directly to the smooth flow of procedures between the clinic, laboratory, and urine monitoring areas while maintaining a clean, safe, and well-organized PK processing environment.

Responsibilities

  • Collect and harvest plasma, serum, and other required laboratory specimens from study subjects in strict accordance with protocol specifications.
  • Monitor the collection of urine and, when required, fecal specimens from subjects participating in clinical studies to ensure compliance with study procedures.
  • Assist with urine collection from subjects as needed, following established clinical and laboratory guidelines.
  • Collaborate with coordinators and floor technicians (phlebotomists) to support the smooth and orderly flow of procedures across the clinic, laboratory, and urine monitoring areas.
  • Organize, label, and process PK samples in the designated PK processing area, ensuring accuracy, traceability, and timely handling.
  • Complete all required study documentation accurately and in a timely manner, including logs, forms, and electronic records as defined by the protocol.
  • Undergo training and demonstrate competency on special laboratory and clinical equipment as required by specific study protocols.
  • Maintain all procedures and processing areas in a neat, clean, and organized condition, following good laboratory practices and safety guidelines.
  • Follow established quality control procedures to ensure the integrity and reliability of collected and processed specimens.
  • Perform other related duties as assigned to support clinical and laboratory operations, which may include limited assistance with on-floor clinic activities when needed.

Essential Skills

  • Previous laboratory experience comparable to approximately 1 year, providing the knowledge, skills, and abilities to perform specimen collection and processing tasks.
  • Demonstrated proficiency in specimen processing, including handling, labeling, and organizing blood and urine samples.
  • Skill in pipetting and other basic laboratory techniques used in clinical research and PK sample processing.
  • Experience working in a clinical research or laboratory environment with an understanding of protocol-driven procedures.
  • Knowledge of quality control practices in a laboratory setting to ensure accurate and reliable sample handling.
  • Ability to work collaboratively with phlebotomists, coordinators, and other clinical staff to support coordinated study workflows.
  • Strong attention to detail and accuracy in completing study documents and maintaining sample records.
  • Ability to learn and operate special laboratory equipment and follow study-specific training requirements.
  • High / secondary school diploma or equivalent and relevant formal academic or vocational qualification.

Additional Skills & Qualifications

  • Technical positions may require a relevant technical or laboratory certificate.
  • Experience in clinical research units, particularly Phase I settings with healthy volunteer studies, is beneficial.
  • Familiarity with pharmacokinetic (PK) sample collection and processing workflows is an advantage.
  • Comfort working with blood, urine, and fecal specimens in a clinical research environment.
  • Strong organizational skills to maintain an orderly PK processing area and manage multiple study tasks.
  • Ability to adapt to changing study needs and perform additional duties as assigned in a fast-paced clinical research setting.

Job Type & Location

This is a Contract position based out of Las Vegas, NV.

Pay and Benefits

The pay range for this position is $21.00 - $21.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Las Vegas,NV.

Application Deadline

This position is anticipated to close on Aug 28, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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