Clinical Research Associate Saint Louis University

  • Saint Louis University
  • Saint Louis, Missouri
  • Full Time

Under general supervision, the clinical research associate (CRA) will be responsible for oversight of clinical trials for the SLU School of Medicine. Responsibilities include screening, recruiting and enrolling subjects, conducting subject research visits, providing technical and administrative expertise in the preparation and administration of investigational products (imaging & therapy) in research subjects, data collection and data entry,A detailed source documentation, maintenance of study documents, and review of budgets in coordination with the Clinical Trials Office . The CRA will liaise with core offices including the Clinical Trials Office, SLU Institutional Review Board, SLU Radiation Safety Committee & SSM Research Compliance OfficeA as well as industry sponsors and associated CROs/vendors. The position will require the ability to collaborate with departmental as well as non-departmental team members and other research professionals in a manner consistent with St. Louis University's core values.

PRIMARY JOB RESPONSIBILITIES :

  • Screens, recruits and enrolls patients into research studies in accordance with good clinical practice.

  • Schedules and conducts research study visits.

  • Provides technical and administrative expertise in the preparation and administration of investigational products.

  • Records and documents study visits utilizing ALCOA+ principles.

  • Data entry and query resolution.

  • Maintains accurate and complete study documents.

  • Liaise withA Clinical Trials Office, SLU Institutional Review Board, SLU Radiation Safety Committee & SSM Research Compliance Office.

  • Liaise with industry sponsors, CROs and vendors.

  • Attends meetings, performs other duties as assigned.

  • Performs other duties as assigned.

KNOWLEDGE, SKILLS, AND ABILITIES :

  • Knowledge of regulations and guidelines related to clinical research

  • Working knowledge of clinical research terminology and multiple medical conditions

  • Knowledge of GE Centricity, EPIC, Clinical Conductor CTMS and other University Electronic Data Systems

  • Ability to efficiently operate computer software for Electronic Health Record and Practice Management Systems

  • Strong interpersonal and customer service skills

  • Excellent time management, organizational and multitasking skills

  • Ability to maintain confidentiality

MINIMUM QUALIFICATIONS :

  • Bachelors degree; supplemented with two (2) years of related work experience

PREFERRED QUALIFICATIONS :

  • CNMT Certification

Job ID: 483118922
Originally Posted on: 6/28/2025

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