Job detail

Research Assistant (PRN)

Evolution Research Group

#Phlebotomy #Medical Terminology #FDA Regulations #Night Shift #Specimen Processing #Clinical Research #GCP #Psychiatry #Neuroscience #Clinical Trials #ECG #Neurology

Unknown On Site 0-2 yrs$18 - $22 / HOURPosted 3 days ago

Location

Miami, Florida

Salary

$18 - $22 / HOUR

Quick overview

The Research Assistant is responsible for executing clinical trial protocols, including performing vitals, ECGs, and phlebotomy. They also manage data entry, lab kit inventory, and the processing and shipping of specimens.

Requirements summary

Candidates should have a high school diploma, though a college degree and one year of clinical experience are preferred. Knowledge of GCP, ICH guidelines, and medical terminology is required, along with a willingness to work night shifts.

high schoolbachelor degreeAttention To DetailWritten CommunicationVerbal CommunicationInterpersonal CommunicationPhlebotomyMedical TerminologyData EntryOrganization SkillsSpecimen ProcessingGood Clinical PracticeFDA RegulationsICH Guidelines

Job description

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 Research Assistant will ensure compliance with protocol and overall clinical objectives. In executing these position responsibilities, the Research Assistant is guided FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

Responsibilities

Prepare source documents for study visits.
Perform vitals, ECGs, and phlebotomy.
Data Entry from patient visit
Manage lab kit inventory.
Ship and process specimens
Undertake protocol trainings as assigned.
General office tasks such as filing, copying, and scanning.
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

Education and experience
1 year of clinical experience is preferred.
High School Diploma or its equivalent; College degree preferred.
Requirements
Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
Knowledgeable in medical terminology
Organization skills required.
Good organizational and interpersonal skills
Attention to detail.
Excellent communication skills (interpersonal, written, verbal)
Must be willing to work a NIGHT SHIFT