COMPANY OVERVIEW

ClinSmart, LLC is a full-service contract research organization dedicated to providing a wide range of services that help clients achieve their clinical development goals. With a focus on personalized service and an experienced team, ClinSmart stands out in the industry for its responsiveness and cost-effectiveness.

SUMMARY

Currently seeking an experienced Clinical Research Associate (CRA) for an opportunity to monitor a clinical psychology trial at a prestigious University setting in Connecticut.

POSITION SUMMARY

The CRA will be responsible for monitoring a Clinical Schizophrenia trial and managing all aspects of site start-up, maintenance, Interim and close out activities.

DESIRED SKILLS AND EXPERIENCE

• Verifiable psychology study monitoring experience within the past 2 years
• Strong understanding of clinical psychology trials including medical terminology and scientific rationale
• Understanding of tools/scales used to measure symptoms of schizophrenia
• Excellent interpersonal and written communication skills with an orientation to detail
• Solid knowledge of Good Clinical Practice (GCP) regulations, ICH guidelines and Local Regulations
• Computer proficient with database platforms to verify accuracy and completeness of data collected at investigative site

EDUCATION AND EXPERIENCE:

• BS/BA in Life Science or Nursing (or equivalent foreign education / experience) required
• Minimum of 3 years CRA experience within the pharmaceutical or biotechnology industry
  Job Types: Part-time, Contract
  Pay: From $75.00 per hour
  Expected hours: 20 – 35 per week

Application Question(s):

• Do you have experience with Schizophrenia patient care studies?

Education:

• Bachelor’s (Required)

Experience:

• Clinical Research : 3 years (Required)
• Schizophrenia patient care studies: 3 years (Required)

License/Certification:

• Driver’s License (Required)

Work Location: On the roa

• Conduct monitoring visits according to the Monitoring Plan
• Monitor adherence to the study protocol and report any violations
• Report serious adverse experiences (SAEs) to the Safety Officer
• Collect appropriate Investigator documentation and maintain files throughout the trial
• Track drug and lab shipments and monitor stability and storage conditions
• Document accountability for pertinent clinical trial materials