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Part-Time Clinical Research Observers

About Gateway Clinical Trials

Gateway Clinical Trials is a private clinical research company headquartered in O’Fallon, Illinois, with an expanding presence in the St. Louis area. We are growing our research program into new therapeutic areas, including psychiatry, and are looking for motivated individuals to join our team for upcoming clinical trials.

Position Overview

We are seeking several part-time Clinical Research Observers to support upcoming psychiatry clinical trials involving patients with dementia-related agitation and psychosis associated with Alzheimer’s disease.

This is an excellent opportunity for graduate students, gap-year students, or individuals interested in psychology, neuroscience, medicine, or clinical research to gain hands-on experience in psychiatry research.

Clinical Research Observers will provide study-related observation, monitoring, and support during active trial periods. We are looking for dependable, detail-oriented individuals who can commit to a consistent schedule throughout a designated 21-day study period.

Please note: These are contract opportunities tied to upcoming studies. Start dates will depend on study activation and participant enrollment, and candidates should be available to commit to a 21-day observation period with approximately 2–4 weeks’ advance notice.

Scheduling Requirements

We are primarily seeking individuals who can consistently cover one of the following schedules for the full 21-day observation period:

  • Morning/Day Shift: 6:00 AM – 2:00 PM 
  • Evening Shift: 6:00 PM – 10:00 PM 

Schedules may include weekdays and weekends. Our ideal candidates will be able to commit to the same shift consistently throughout the study period to promote continuity of observation and participant support.

Key Responsibilities

  • Provide study-related observation and monitoring during active clinical trial periods. 
  • Support study staff with observation-related activities in accordance with study protocols and site procedures. 
  • Maintain accurate and timely documentation of assigned observations, as required. 
  • Follow study protocols, confidentiality requirements, and applicable research procedures. 
  • Communicate relevant observations and concerns to designated study personnel. 
  • Maintain professionalism and respect when interacting with study participants and clinical staff. 

Qualifications

  • Interest in psychiatry, psychology, neuroscience, medicine, nursing, or clinical research. 
  • Strong attention to detail and ability to follow study procedures. 
  • Dependability and a strong commitment to the assigned schedule. 
  • Professional communication skills and respect for participant confidentiality. 
  • Ability to work independently while following the direction of the study team. 
  • Availability to commit to a 21-day observation period with approximately 2–4 weeks’ notice. Graduate students, gap-year students, and candidates considering careers in healthcare, mental health, or clinical research are encouraged to apply. 
  • Prior clinical research experience is welcome but not required.

Why Join Gateway Clinical Trials?

  • Gain hands-on exposure to psychiatry clinical research. 
  • Build relevant experience for future academic, clinical, or research careers. 
  • Work alongside a team involved in expanding clinical research opportunities in the St. Louis area. 
  • Earn $22.50–$25.00 per hour in a part-time contract role. 

Pay: $22.50 - $25.00 per hour

Expected hours: 1.0 – 40.0 per week

Work Location: In person