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Research Assistant - DAY SHIFT

Evolution Research Group
Posted 3 months ago, valid for 21 days
Location

Doral, FL, US

Salary

$19 - $25 per year

Contract type

Part Time

Paid Time Off

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Sonic Summary

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  • Evolution Research Group (ERG) is a leading neuroscience clinical development company founded in 2014, specializing in Phase I–IV clinical trial execution.
  • The Research Assistant role involves ensuring compliance with clinical protocols and performing tasks such as data entry, vitals, ECGs, and phlebotomy.
  • Candidates should have at least 1 year of clinical experience, with a high school diploma required and a college degree preferred.
  • The position requires knowledge of regulatory requirements, Good Clinical Practices (GCP), and strong organizational and communication skills.
  • Salary details are not explicitly mentioned, but ERG offers competitive benefits including medical coverage, a matching 401(k), and paid time off.

About Company:

Evolution ResearchGroup (ERG) is dedicated to delivering high-quality Phase I–IV clinical trialexecution to help sponsors bring lifesaving and life-enhancing therapies tomarket quickly and safely. Founded in 2014, ERG has grown into a leadingneuroscience 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 andcontinues 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) 



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