PK Lab Technician (3p-11p)

Ergclinical; Miami (FL); On-site; USD 24,796 - 33,062; Full time

Job summary

Evolution Research Group in Miami, FL is seeking a Lab Assistant to perform clinical and pharmacokinetic specimen collection and processing for Phase 1 trials, mainly healthy volunteers. Duties include assisting the Lab Manager with samples, with occasional clerical/data-entry tasks. Hours vary and may require weekends or early/late shifts.

The role emphasizes safety and accuracy in handling specimens and complying with GCP/ICH guidelines. Training provided where needed.

Qualifications

• Phlebotomy Technician certification or at least 6 months phlebotomy experience.
• Clinical Research experience preferred but not required.
• BLS/ACLS certification preferred but not required.
• Knowledge of GCP and ICH guidelines.
• Medical terminology knowledge.
• Basic computer skills (Word, Excel; Study Manager).

Responsibilities

• Monitor urine collection temperatures and 24-hour collections.
• Maintain clean, stocked sample collection area.
• Notify staff of abnormal results or incidents.
• Act as courier to Pharmacokinetic lab for specimens.
• Label PK/PD collection tubes.
• Ensure participant comfort and safety during shifts.
• Perform safety lab requisitions and sample send-outs.
• Role may expand to meet organizational needs.

Skills

Medical terminology

Regulatory knowledge (GCP/ICH)

Computer literacy (Word, Excel)

Education

Phlebotomy Technician certification

Tools

Study Manager

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 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 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.
• 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).