Clinical Research Asst.

EVOLUTION RESEARCH GROUP
Bellaire, TX Other
POSTED ON 12/5/2022 CLOSED ON 1/3/2023

What are the responsibilities and job description for the Clinical Research Asst. position at EVOLUTION RESEARCH GROUP?

Job Details

Job Location:    LOC009 HDR First Surgical Hospital - Bellaire, TX
Salary Range:    Undisclosed

Research Assistant-PRN

Title: Research Assistant-PRN

Location: Bellaire, TX

 

Job Description:

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

 

Responsibilities:

  • Prepare source documents for study visits
  • Perform vitals, ECG’s, 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

 

Skills and Qualifications:

  • Education and experience
    • 1 year of clinical experience is preferred.
    • High School Diploma or its equivalent; College degree preferred
  • Requirements
    • Understands 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)
    • Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as RealTime)


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