Clinical Research Associate

2 weeks ago


Springfield, Missouri, United States QPS, LLC Full time
Position Overview

The Clinical Research Technician role provides a dynamic work environment within the pharmaceutical research sector. This position is primarily tasked with overseeing study participants and ensuring that clinical trials are executed, documented, and reported in accordance with established study protocols. Each day presents unique challenges and responsibilities, with hours scheduled flexibly between 0-29 hours per week. Key responsibilities include:

  • Comprehending and interpreting study documentation, timelines, and sponsor expectations.
  • Managing the check-in and check-out process for study participants while monitoring their adherence to study protocols, safety, and any adverse events.
  • Conducting essential study tasks such as recording meal times, taking vital signs, and documenting results.
  • Reviewing raw data to confirm its accuracy.
  • Assisting in the supervision of events to ensure timely completion of studies in line with Standard Operating Procedures (SOPs) and protocols.
  • Ensuring cleanliness and organization of clinical and study-related areas.

Qualifications

  • Exceptional customer service abilities.
  • Meticulous attention to detail.
  • Willingness to work on weekends is a plus.
  • Flexibility in scheduling is essential.

QPS, LLC is committed to providing equal employment opportunities (EEO) to all employees and applicants without regard to race, color, religion, sex, national origin, age, disability, or genetics. This commitment extends to all employment terms and conditions, including recruitment, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.



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