Research Assistant (PRN, 11p-7a)

Posted Yesterday
Be an Early Applicant
Miami, FL, USA
In-Office
16-23 Hourly
Junior
Healthtech
The Role
Supports Phase I–IV clinical trials by preparing study documents, performing vital signs, ECGs, and phlebotomy, entering patient visit data, managing lab inventory, processing and shipping specimens, and completing protocol training. The role also includes office administration and requires adherence to FDA regulations, GCP, ICH guidelines, and company procedures. Night-shift availability is required.
Summary Generated by Built In

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

Skills Required

  • High school diploma or equivalent
  • One year of clinical experience
  • College degree
  • Understanding of regulatory requirements, Good Clinical Practices, and ICH guidelines
  • Knowledge of medical terminology
  • Strong organizational skills
  • Good interpersonal skills
  • Attention to detail
  • Excellent written and verbal communication skills
  • Willingness to work night shift
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The Company
HQ: Edison, New Jersey
175 Employees
Year Founded: 2014

What We Do

ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with an expertise in early and late stage neuroscience drug development. With 21 wholly owned clinical sites and 5 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 340+ in-patient beds, a large and growing database of patients suffering from mental illness, neurological disorders, sleep disorders, addictions, Acute and Chronic Pain, diabetes and other illnesses as well as normal healthy volunteers who participate in trials for the advancement of medicine. With access to over 32 million patients/subjects and 5000 + completed trials, ERG continues to grow its capabilities and expand into indications where there are tremendous unmet medical needs in the United States and globally. The ERG portfolio of sites we own consists of Woodland International Research Group, Woodland Research Northwest, Midwest Clinical Research, Pacific Research Network, Clinical Pharmacology of Miami, Brain Matters Research, Neuropsychiatric Research Center, Richmond Behavioral Associates, Finger Lakes Clinical Research, Endeavor Clinical Trials, and HD Research, all supported by an industry leading centralized infrastructure located in New Jersey. ERG offers consulting services to pharmaceutical and CRO clients, including access to key opinion leaders in Schizophrenia, Pain, Alzheimer’s disease, Sleep Disorders, Depression, Hepatic/Renal Impairment, Podiatry and Clinical Pharmacology. This includes Rater Training Services, Centralized Data Services (ECG, PSG, EEG, qEEG, Actigraphy), Medical Writing Services, Study Feasibility and Site Recommendation ERG also offers general consulting in study design, protocol review and budget planning, vendor resources, Scientific Advisory Board Planning and Implementation, study feasibility and site recommendations.

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