PK Lab Technician

Evolution Research Group; Miami (FL); On-site; USD 25,000 - 33,000; Full time

Benefits offered by this job

Medical and dental coverage

401(k) matching

Paid time off

Job summary

Evolution Research Group in Miami, FL is seeking a Lab Assistant to support Phase 1–IV clinical trials. The role involves collecting and processing pharmacokinetic specimens from healthy volunteers, with emphasis on accuracy, safety, and timely data entry.

Hours are project-dependent and may include weekends or off-hours. Qualified candidates will have a Phlebotomy Technician certification (or at least six months of phlebotomy experience), familiarity with GCP guidelines, and basic computer

Qualifications

• Phlebotomy Technician certification or 6+ months phlebotomy experience.
• Clinical research experience preferred.
• Familiar with GCP/ICH guidelines and medical terminology.

Responsibilities

• Monitor urine and 24-hour specimen collections.
• Assist Lab Manager with processing laboratory samples.
• Perform clerical and data entry duties as needed.
• Ensure sample collection area is clean and stocked.
• Follow safety protocols to protect participants.

Skills

Phlebotomy

Clinical Research

Regulatory knowledge (GCP/ICH)

Medical terminology

Education

Phlebotomy Technician Certification

Tools

Study Manager

Word

Excel

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Full Time CPMI-Clinical Pharmacology Miami, Miami, FL, US

Salary Range: $18.00 To $24.00 Hourly

About Company:

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.

Why join us?

We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.

Job Description:

The Lab Assistant will perform basic and complex clinical and pharmacokinetic specimen collection and processing (upon assignment) for Phase 1 clinical trials, primarily healthy paid volunteers. Duties will primarily focus on assisting the Lab Manager in processing laboratory samples but will also include clerical and data entry duties. Hours are project dependent and sometimes require weekends and/or very early or late hours.

Responsibilities:

• Monitorurine collection temperatures, as assigned.
• Monitor24-hour specimen collections (i.e., urine, feces), as assigned.
• Maintain sample collection area clean and stocked with all necessary supplies.
• Notify appropriate staff of abnormal results while collecting specimens, adverse events, or unusual incidents.
• Act as courier to Pharmacokinetic laboratory for collected specimens.
• Assure minimal discomfort for study participants while performing all duties.
• Maintain safety and well-being of study participants during assigned shift.
• Safety lab requisition creation and sample send out to the local labs.
• Labeling of PK/PD collection tubes
• Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.

Skills and Qualifications:

• Certification as a Phlebotomy Technician and/or a minimum of six months experience working as a phlebotomist at a medical facility.
• Clinical Research experience preferred but not required.
• BLS and/or ACLS certification preferred but not required.
• Understandregulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
• Knowledgeable in medical terminology
• Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)