Research Specialist I

Texas A&M University SystemHouston, TX
Onsite

About The Position

The Research Specialist I, under general supervision, compiles and reviews data and metadata. Computes projections and performs analysis and tests. Supports Principal Investigator and Research Personnel in the day-to-day conduct of clinical research activities.

Requirements

  • Bachelor’s degree or equivalent combination of education and experience.
  • Four years of related experience in a specialized and relevant field of research.
  • Ability to multitask and work cooperatively with others.
  • Knowledge of word processing, spreadsheet, database, and presentation applications.
  • Interpersonal and communication skills.
  • Planning and organization skills.
  • Familiarity with appropriate laboratory and/or technical equipment.
  • Ability to effectively utilize a computer and applicable software.
  • Attention to detail.
  • Knowledge of FDA regulations, Good Clinical Practice (GCP), HIPAA, and human subject protections.
  • Proficient computer skills, including Microsoft Office Suite and electronic medical record (EMR) systems.

Nice To Haves

  • Experience working in a physician practice, hospital, oncology clinic, or other healthcare environment
  • Experience with electronic data capture (EDC) systems and regulatory documentation
  • Current CITI Human Subjects Protection (HSP) training certification or equivalent, or the ability to obtain certification upon hire

Responsibilities

  • Compiles and reviews data and metadata.
  • Collects samples and measurements for experiments.
  • Implements and maintains data collection and summarization of clinical trials.
  • Computes projections.
  • Performs analysis and tests.
  • Makes and records observations and scientific measurements.
  • Assist with collection, processing, shipping, and tracking of research specimens.
  • Assist in preparing for sponsor monitoring visits, audits, and inspections.
  • Track enrollment, follow-up, and protocol compliance.
  • Maintain HIPAA compliance and participant confidentiality.
  • Screen potential participants for eligibility according to study protocols.
  • Schedule participant visits and study-related appointments.
  • Assist with participant recruitment and retention
  • Enter study data into electronic databases and EMRs.
  • Utilizes summarized results in scientific and/or clientele-oriented publications.
  • Prepares and writes proposals to funding agencies and maintains financial accounts related to research projects.
  • Prepare study materials and participant packets.
  • Maintain research records, regulatory binders, and study documentation.
  • Executes assigned protocols in accordance with research-governing entity requirements, including but not limited to Sponsor, FDA, and IRB requirements
  • Trains undergraduate and/or graduate students and other laboratory, technical or clinical staff involved in research.
  • Develops and maintains training materials for external users.
  • Monitors and tracks all lab-related supplies and inventory levels.
  • Purchases lab supplies, equipment, and services for the project.
  • Assists with Rural Oncology Grant invoice processing based on the sub-awardee needs.

Benefits

  • Medical, prescription drug, dental, vision, life and AD&D, flexible spending accounts, and long-term disability insurance with Texas A&M contributing to employee health and basic life premiums
  • 12-15 days of annual paid holidays
  • Up to eight hours of paid sick leave and at least eight hours of paid vacation each month
  • Automatic enrollment in the Teacher Retirement System of Texas
  • Free exercise programs and release time
  • All employees have access to free LinkedIn Learning training, webinars, and limited financial support to attend conferences, workshops, and more
  • Educational release time and tuition assistance for completing a degree while a Texas A&M employee
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