PK Lab Technician (PRN)

Evolution Research Group; Miami (FL); On-site; USD 36,000 - 48,000; Full time

Benefits offered by this job

Medical and dental coverage

401(k) matching

Paid time off

Job summary

Evolution Research Group is seeking a Lab Assistant to support Phase I–IV clinical trials with specimen collection and processing. The role involves assisting the Lab Manager, monitoring specimen collections, and maintaining a compliant, efficient lab environment.

Weekend and extended hours may be required. The position emphasizes phlebotomy duties, adherence to GCP/ICH guidelines, and basic data-entry tasks, with opportunities to contribute to cutting-edge research at ERG’s neuroscience-focused

Qualifications

• Phlebotomy Technician certification or 6+ months phlebotomy experience.
• Clinical Research experience preferred.
• BLS/ACLS certification preferred.
• Knowledge of GCP/ICH guidelines and regulations.
• Medical terminology is essential.
• Basic computer skills (Word, Excel) and lab software familiarity.

Responsibilities

• Monitor urine collection temperatures and 24-hour specimen collections as assigned.
• Assist Lab Manager in processing samples and maintaining the collection area.
• Perform clerical/data-entry duties as required.
• Ensure safety and comfort of study participants during shifts.
• Serve as courier to the Pharmacokinetic laboratory for specimens.
• Maintain clean, stocked collection areas and proper labeling of tubes.
• Report abnormal findings and assist with documentation and requisitions.

Skills

Medical terminology

GCP/ICH knowledge

Computer basic skills

Phlebotomy knowledge

Education

Phlebotomy Technician certification

Tools

Study Manager

Job description

Overview

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 including 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

• Monitor urine collection temperatures, as assigned.
• Monitor 24-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 the 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.

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.
• Understand regulatory 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).