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Research Assistant-PRN RA

Job in Bellaire, Harris County, Texas, 77401, USA
Listing for: Evolution Research Group
Full Time, Seasonal/Temporary, Per diem position
Listed on 2025-12-31
Job specializations:
  • Research/Development
    Research Assistant/Associate, Clinical Research
  • Healthcare
    Clinical Research
Job Description & How to Apply Below

Join to apply for the Research Assistant-PRN RA role at Evolution Research Group
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About Us

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. Competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.

We are seeking a highly motivated PRN Research Assistant (RA) to join our team. You will be responsible for assisting with research studies, collecting and analyzing data, and ensuring compliance with study protocols. The Research Assistant will ensure compliance with protocol and overall clinical objectives. In executing these position responsibilities, the Research Assistant is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

Responsibilities
  • Assist with research studies by collecting and analyzing data
  • Ensure compliance with study protocols and regulations
  • Maintain accurate and complete records of research activities
  • 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
  • Perform general office tasks such as filing, copying, and scanning
  • Additional responsibilities as required by the evolving needs of the organization
Minimum Qualifications
  • High School Diploma or its equivalent;
    College degree preferred
  • 1 year of clinical experience is preferred
  • Strong organizational and communication skills
  • Ability to work independently and as part of a team
  • Attention to detail and accuracy
Preferred Qualifications
  • Experience with clinical research studies
  • Knowledge of regulatory requirements for research studies
  • Knowledgeable in medical terminology

Seniority level:
Entry level

Employment type:

Full-time

Job function:
Research, Analyst, and Information Technology

Industries:
Research Services

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