Research Specialist I

About the role

This position will report to IBT located in downtown Houston, Texas. The employee will be located at a Non TAMU private clinical office in Corpus Christi. May have to work on the weekends and/or after normal hours. May travel as required. Please note: This position is grant funded; future employment may be contingent upon future funding.

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

Qualifications

• Required Education And Experience
  • Bachelor’s degree or equivalent combination of education and experience
  • Four years of related experience in a specialized and relevant field of research
• Preferred Qualifications
  • 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
• Knowledge, Skills, And Abilities
  • 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