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Clinical Research Coordinator

Job in Denton, Denton County, Texas, 76205, USA
Listing for: Revival Research Institute, LLC
Full Time, Seasonal/Temporary position
Listed on 2026-01-01
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research, Research Assistant/Associate
Salary/Wage Range or Industry Benchmark: 65000 - 80000 USD Yearly USD 65000.00 80000.00 YEAR
Job Description & How to Apply Below

Clinical Research Coordinator at Revival Research Institute, LLC

Location: Frisco, TX

Salary: $65,000.00 – $80,000.00

Seniority level: Entry level

Employment type: Full-time

Job function: Research, Analyst, and Information Technology

As Revival Research Institute is growing, we are looking to add qualified professionals to our team. We are seeking a full‑time Clinical Research Coordinator with a minimum of 1 year of clinical experience. A strong interest in the Clinical Research field would be an excellent fit for our entry‑level position; however, this interest and background is not necessary. The ideal candidate is detail‑oriented, organized, and motivated to learn new things.

Responsibilities
  • Participate in research participant screening, recruitment, and enrollment. Consent and conduct research visits for data collection, minimal risk trials with oversight. Responsible for collecting, processing, and shipping research specimens, where applicable.
  • Document study related information in case report forms or electronic data capture systems, handle data queries, and participate in monitoring visits. Obtain, review, and maintain source documents.
  • Maintain organization of all trial related documents and correspondence. Implement quality control and assurance methods.
  • Communicate with study sponsors, research team, and the Institutional Review Board. Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting.
  • Maintain professional and technical knowledge about clinical trials.
  • Communicate with research participants/families, protect patient confidentiality.
Preferred Qualifications
  • Education/Training:
    Bachelor’s degree in a health‑related field with 1–2 years relevant clinical experience OR Master’s degree in a medical‑related field with no research experience. Individuals with more experience are preferred; if qualifications exceed entry level, higher positions are available.
  • Phlebotomy skills preferred.
  • Psychology experience with knowledge of psychiatric rating scales preferred.
  • Certifications, Licensures, and Registrations:
    National Certification (CRA or ACRP), BLS Certification.
  • Additional Qualifications:

    Expert database and computer skills:
    Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Knowledge of FDA Regulations and Good Clinical Practice.
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