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Phlebotomy Technician

Actalent

Miami, FLContract$18–20/hrSeen 2 days agoSeen in employer's feed 2 days ago

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At a glance

Compensation
$18–20/hr
Location
Miami, FL
Schedule
Contract
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Phlebotomy CertificateMedical Assistant Certificate

Job overview

Actalent seeks Phlebotomy Technicians to support clinical research studies in Miami, performing specimen collection, vital sign monitoring, and documentation while adhering to protocols, SOPs, and regulatory standards. The role involves coordinating with labs, managing sample shipping, and assisting recruitment, requiring strong collaboration in a multidisciplinary environment.

Skills & qualifications

RequiredNice to have

Skills

Phlebotomy CertificateMedical Assistant CertificateFamiliarity With Clinical Research ProtocolsExperience Recording Equipment TemperaturesKnowledge of Shipping RegulationsCollaborative Teamwork

Qualifications

Minimum of Two Years Active Phlebotomy ExperiencePhlebotomy CertificateMedical Assistant Certificate

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Paid Time Off

Full job description

Actalent is Hiring a Team of Phlebotomy Technicians!! All Shifts Available!

Job Description

The Screening Research Technician plays a key role in supporting clinical research studies by performing screening procedures, processing biological specimens, and ensuring strict adherence to study protocols, standard operating procedures, and regulatory requirements. This position focuses on accurate specimen handling, vital sign collection, documentation, and coordination with clinical and laboratory teams to ensure the integrity and reliability of study data.

Responsibilities

  • Review study protocols prior to the initiation of each study to understand all screening and specimen processing requirements.

  • Attend protocol training meetings to review specimen processing procedures and confirm the availability of required supplies.

  • Coordinate services with any central laboratory involved in the study to ensure timely and accurate processing of samples.

  • Perform study procedures, including vital signs and sample collection, in full compliance with study protocols and standard operating procedures (SOPs).

  • Notify the Screening Nurse of any vital sign or laboratory parameter that may exclude a volunteer from participation in a study.

  • Complete source documents in accordance with Good Clinical Practice (GCP) and Good Documentation Practice (GDP) standards, ensuring accuracy and completeness.

  • Comply with all relevant SOPs related to clinical research, specimen handling, and documentation.

  • Perform quality control checks for laboratory requisitions to verify accuracy and completeness before submission.

  • Report events involving damage or loss of samples, spillage incidents, or employee injury, following established incident reporting procedures.

  • Record the temperature of all freezers and refrigerators on the appropriate temperature logs on a daily basis to maintain sample integrity.

  • Verify that all biohazardous materials are disposed of appropriately and ensure proper labeling and preparation of biohazardous waste for transport.

  • Prepare specimens for shipping and adhere to all regulations governing the shipment of biological samples.

  • Arrange overnight or express shipping of specimens and maintain accurate and complete shipping documentation.

  • Receive and sort all laboratory test results for review by Investigators and clinical staff.

  • Ensure that all laboratory results for potential volunteers have been received and reviewed prior to their utilization in a study.

  • Perform vital sign measurements for volunteers and study participants as required by study protocols.

  • Perform blood collection, vital signs, and other study procedures based on Screening and Clinic scheduling needs.

  • Assist the recruitment team when required, supporting volunteer screening and enrollment activities.

  • Assist with other duties as assigned to support the smooth operation of the clinical research unit.

Additional Skills & Qualifications

  • Phlebotomy certificate and/or Medical Assistant certificate.

  • Minimum of two years of active phlebotomy and laboratory procedures experience.

  • Familiarity with clinical research protocols and SOP-driven environments.

  • Experience recording and monitoring equipment temperatures, particularly freezers and refrigerators used for specimen storage.

  • Knowledge of regulations and best practices for shipping biological samples.

  • Ability to work collaboratively in a multidisciplinary clinical research setting.

Work Environment

This role is based in a clinical research and laboratory setting that focuses on the screening and evaluation of study volunteers. The Screening Research Technician works with biological specimens, including blood samples, and uses equipment such as vital sign monitors, freezers, refrigerators, and shipping materials for biological samples.

Job Type & Location

This is a Contract position based out of Miami, FL.

Pay and Benefits

The pay range for this position is $18.00 - $20.00/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 Miami,FL.

Application Deadline

This position is anticipated to close on Oct 14, 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 [email protected] 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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