Health Plan Nurse Coordinator I

ERA Health Research

Midland, TXFull-timePosted May 2, 2026

Behavioral Health Market Context

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Benefits

Pay and benefitsPay Range: $42.00/hourly - $52.00/hourlyPay is based upon candidate experience and qualifications, as well as market and business considerationsERA Health Research provides eligible employees with an opportunity to enroll in a comprehensive benefits package which includes:Medical, dental, and vision insuranceFlexible Spending Account (FSA) and Health Savings Account (HSA) options401k Retirement Savings PlanPaid time off (PTO) starting at10 days per year and 1 hour of sick leave for every 40 hours worked2 Floating Holidays per year6 more items(s)

Qualifications

  • A valid and current Registered Nurse (RN) license in Texas is a mandatory requirement for this position
  • Applications without a Texas RN license will not be considered
  • Current Registered Nurse (RN) license in the applicable state
  • 1 year of Nurse experience
  • Basic understanding of medical terminology
  • Strong attention to detail and organizational skills
  • Ability to follow detailed instructions and protocols
  • Good written and verbal communication skills
  • Proficient with basic computer software (MS Office)
  • ~ Experience in Clinical research or a relevant clinical setting
  • 7 more items(s)

Responsibilities

  • This role is an entry-level role focused on learning the fundamental principles of clinical research coordination under close supervision
  • This individual supports the research team by performing routine data collection and administrative tasks, ensuring compliance with protocols and regulatory standards
  • Assist with patient screening and recruitment for clinical trials
  • Support the informed consent process under the direct supervision of a senior CRC or manager
  • Perform basic clinical data entry and management into Electronic Data Capture (EDC) systems
  • Assist with scheduling patient visits and procedures
  • Help with the preparation of source documents and study binders
  • Maintain inventory of study supplies and equipment
  • Handle processing and shipment of lab samples following IATA/DOT regulations (with training)
  • Attend study meetings and complete required training (GCP, HIPAA, Protocol-specific)
  • Perform nursing assessments and conduct protocol-related procedures (vitals, ECGs, infusions, pharmacokinetic sampling, etc.)
  • Administer investigational products (drugs, devices, biologics) per protocol
  • Monitor patient responses to investigational products and provide clinical care
  • Assess, document, and report Adverse Events (AEs) and Serious Adverse Events (SAEs) to the PI and sponsor
  • Provide patient education and serve as a clinical resource for participants throughout the study
  • In addition to the specific responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager
  • These additional duties will fall within the scope of the role and contribute to the overall success of the team
  • 14 more items(s)


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