Clinical Research Associate Job at Saint Louis University, Saint Louis, MO

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  • Saint Louis University
  • Saint Louis, MO

Job Description

Who is Saint Louis University? Founded in 1818, Saint Louis University is one of the nation's oldest and most prestigious Catholic universities. SLU, which also has a campus in Madrid, Spain, is recognized for world-class academics, life-changing research, compassionate health care, and a strong commitment to faith and service.

JOB SUMMARY :

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, 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 Office 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 with 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 :
  • Bachelor's degree; supplemented with two (2) years of related work experience

PREFERRED QUALIFICATIONS :
  • CNMT Certification

Function

Clinical Research

Scheduled Weekly Hours:
40

Saint Louis University is an equal opportunity/affirmative action employer. All qualified candidates will receive consideration for the position applied for without regard to race, color, religion, sex, age, national origin, disability, marital status, sexual orientation, military/veteran status, gender identity, or other non-merit factors. If accommodations are needed for completing the application and/or with the interviewing process, please contact Human Resources at [click to reveal phone number]314-977-5847 .

Job Tags

Full time, Work experience placement, Work at office,

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