Clinical Research Assistant I

Eastside Research Associates

Midland, TXFull-timePosted Apr 21, 2026

Behavioral Health Market Context

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Benefits

PAY & BENEFITSPay Range: $22.00/hourly - $26.00/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) options401 k Retirement Savings PlanPaid time off (PTO) starting at10 days per year and 1 hour of sick leave for every40 hours worked2 Floating Holidays per year6 more items(s)

Qualifications

  • Bachelor's degree in Science , Healthcare, other related discipline
  • Strong attention to detail and commitment to accuracy in data entry and record-keeping
  • Excellent organizational, time management, and multitasking abilities
  • Effective written and verbal communication skills
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook)
  • Ability to work collaboratively in a team-oriented, onsite environment
  • A willingness to learn and perform basic clinical procedures (training provided)
  • 4 more items(s)

Responsibilities

  • The Clinical Research Assistant I will play a critical role in supporting the operational and administrative aspects of clinical trials, ensuring compliance with research protocols, and contributing to the accurate collection of study data
  • The ideal candidate is a detail-oriented, motivated individual, eager to begin their career in clinical research
  • This is an onsite position requiring direct involvement in daily research activities
  • Provide day-to-day administrative and operational support for ongoing clinical trials
  • Assist with patient screening and recruitment efforts
  • Create, organize, and maintain patient study charts and source documentation
  • Organize, coordinate, and manage lab supplies and study materials
  • Accurately enter patient enrollment data and medical history into Electronic Data Capture (EDC) systems
  • Respond to and resolve data queries from study monitors or sponsors in a timely manner
  • Clinical Procedures (with training):
  • Perform basic clinical procedures as delegated and trained, which may include:
  • Measuring and recording vital signs (blood pressure, heart rate, temperature)
  • Administering nasal swabs
  • Processing and preparing blood samples for shipment
  • Compliance & Collaboration:
  • Assisting ensuring adherence to Standard Operating Procedures (SOPs) and Good Clinical Practice (GCP) guidelines
  • Support the clinical team in obtaining informed consent from patients under direct supervision
  • Establish and maintain positive relationships with internal team members and external vendors/partners
  • In addition to the job 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
  • 17 more items(s)


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