Clinical Laboratory Technician - 2nd Shift

Actalent; Austin (TX); On-site; USD 29,000 - 32,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) retirement plan

Life Insurance

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

PTO / Vacation

Job summary

Actalent in Austin, TX seeks a Clinical Research Technician to support PK sample collection and processing in a Phase I setting. You will work closely with floor technicians and phlebotomists in a small adjacent lab, handling blood and urine samples for healthy subjects during overnight stays.

The role emphasizes protocol adherence, accurate labeling, documentation, and efficient workflow across clinic and lab areas.

Qualifications

• 1+ year of laboratory task experience.

Responsibilities

• Collaborate with floor technicians and phlebotomists to collect and process PK samples.
• Collect, label, and document plasma, serum, and urine specimens per protocol.
• Assist with urine collection and supervise sample handling across clinic, lab, and monitoring areas.
• Complete study documents and logs for each specimen.
• Operate basic lab equipment after training and maintain clean, organized work areas.
• Participate in weekend rotation while not exceeding 40 hours per week.

Skills

Laboratory experience

Pipetting

Centrifuging

Protocol adherence

Attention to detail

Team collaboration

Weekend rotation

Equipment operation

Documentation

Education

High school diploma or equivalent

Certificate in laboratory science

Tools

Pipettes

Centrifuges

Job description

The Clinical Research Technician supports clinical research studies 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. This role focuses on blood and urine sample handling for healthy study participants in an overnight Phase I clinical research environment and helps ensure that all procedures are carried out accurately, efficiently, and in accordance with study protocols.

Responsibilities

• Work collaboratively with floor technicians and phlebotomists to collect, organize, and process PK samples in the designated PK Processing Area of the clinic.
• Collect and harvest plasma, serum, and other required laboratory specimens strictly following protocol specifications and timing requirements.
• Monitor the collection of urine and, when required, fecal specimens from subjects participating in clinical studies, ensuring accurate labeling and documentation.
• Assist with urine collection from subjects as needed to support smooth study operations.
• Collaborate with study coordinators to maintain a smooth and orderly flow of procedures across the clinic, laboratory, and urine monitoring areas.
• Complete all required study documents, logs, and forms accurately and in a timely manner for each specimen and procedure performed.
• Undergo training on special equipment and laboratory instruments as required by study protocols and apply the training in daily work.
• Maintain all procedures and processing areas in a neat, clean, and organized manner, adhering to quality control and safety standards.
• Perform pipetting, centrifuging, and other routine laboratory techniques in accordance with established procedures.
• Support accessioning and proper tracking of samples to ensure accurate identification and chain of custody.
• Follow all protocol-specific instructions for Phase I studies involving healthy subjects in an overnight stay environment.
• Provide occasional assistance on the clinic floor when requested, while primarily focusing on laboratory and sample processing duties.
• Participate in weekend rotation coverage as needed, while ensuring total weekly hours remain within standard full-time limits.
• Perform other related duties as assigned to support study conduct and overall clinic operations.

Essential Skills

• Previous laboratory experience (comparable to at least 1 year) that provides the knowledge, skills, and abilities to perform routine lab tasks and sample processing.
• Proficiency in basic laboratory techniques, including pipetting, centrifuging, and handling blood and urine specimens.
• Ability to follow detailed clinical research protocols and standard operating procedures accurately.
• Strong attention to detail for specimen labeling, documentation, and data entry to maintain sample integrity and study quality.
• Capability to work in a Phase I clinical research environment with healthy subjects participating in overnight stays.
• Effective communication skills to collaborate with floor technicians, phlebotomists, and study coordinators.
• Organizational skills to keep laboratory and processing areas neat, clean, and well-structured.
• Reliability and flexibility to participate in weekend rotation coverage without exceeding 40 hours per week.
• Ability to learn and operate special laboratory equipment after receiving protocol-specific training.
• Commitment to quality control and adherence to safety and cleanliness standards in all laboratory activities.

Additional Skills & Qualifications

• High or secondary school diploma or equivalent, combined with relevant formal academic or vocational qualification.
• Technical positions may require a related certificate in laboratory science, medical technology, or a similar field.
• Experience in clinical research or Phase I units with healthy subjects is beneficial.
• Familiarity with accessioning processes and sample tracking systems is an advantage.
• Understanding of basic chemistry concepts related to specimen handling and processing.
• Ability to work across multiple functional areas, including clinic, lab, and urine monitoring, as study needs require.

Work Environment

This position is based in a large clinical research unit in Austin, TX, with more than 100 beds and a Phase I model focused on healthy subjects participating in overnight stays. The environment is often described as a 'feed and bleed' setting, where scheduled meals and frequent blood draws are integral to study protocols. The Clinical Research Technician primarily works in a small laboratory just off the clinic floor, in the PK Processing Area, handling blood and urine samples and supporting related procedures. Shifts include an early first shift (06:00–14:00), a standard first shift (08:00–16:00), and a second shift (14:00–22:00), with flexibility requested to help cover occasional weekend staffing as part of a rotation that does not push total hours over 40 per week. The work involves standing, moving between the clinic and lab, and using standard laboratory equipment such as pipettes and centrifuges. The facility maintains a clean, organized, and professional atmosphere, with appropriate clinical and laboratory attire required to support safety, hygiene, and compliance with research standards.

Job Type & Location

This is a Contract to Hire position based out of Austin, TX.

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 Austin,TX. Application Deadline This position is anticipated to close on Oct 1, 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 [e-mail] 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.