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Research Screening Specialist - Lincoln, Nebraska

Celerion

Lincoln, NEOnsitePosted 10 days ago$20.00/hour
Full TimeEntry LevelResearch & ScientistCRO
Original posting ↗

Summary

As a Research Screening Specialist, you will work at our Lincoln, Nebraska site. You will be responsible for the preparation and maintenance of all stages of participant activities including screening, training, and evaluations.

Job description

  • Enter and update study information into database systems
  • Collect and organize panelist's paperwork and documentation
  • Develop positive participant communications and relationships

In this entry level role you will work in an office / clinic environment with a team of 10 colleagues all committed to the same mission: assisting in the development of drugs that will touch the lives of family, friends, and people in need around the world.

For this position you may also be required to travel to our Omaha site approximately 1-2 times per week during working hours. This full time position will work mainly Monday-Friday 5:30am-2:00pm.

Requirements

  • Associate's degree in related field preferred but not required
  • One year customer service experience
  • Experience in organizing and managing multiple priorities
  • Excellent oral and written communication skills
  • Organizational skills
  • General knowledge of Microsoft Windows based applications

Benefits

  • Comprehensive Benefit Package

Company overview

Celerion is a global leader in early clinical research and a premier clinical research organization (CRO) specializing in early-phase drug development. Founded in 2010 with roots dating back to 1969, the company operates with over 50 years of experience in conducting clinical trials. Celerion focuses on Phase 1 studies, including first-in-human dose escalation, drug-drug interactions, cardiac safety, bioequivalence, metabolism, and pharmacokinetics in patient populations. The company's name derives from the Latin 'celeritas,' meaning swiftness and speed, reflecting its commitment to accelerating drug development timelines. With more than 1,000 full-time scientific and medical personnel and over 650 clinical beds across global facilities in North America, Europe, and Asia, Celerion provides comprehensive services including clinical pharmacology studies, bioanalytical services, data management, biostatistics, and regulatory support. The company has conducted over 6,000 studies and works with pharmaceutical and biotechnology clients to enable faster, informed decisions in drug development, helping bring new medicines to market more efficiently.

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