Clinical Research Monitoring (CRA)

Benefits

Qualifications

• •High School Diploma/GED required
• •Licensure, Registration and/or Certification Required by Law:
• •Licensure, Registration and/or Certification Required by SJCRH Only:
• •Bachelor's degree in relevant area required
• •Minimum Requirement: 2+ years of experience in carrying out research preferably in healthcare settings
• •Experience managing cross-functional communication, including liaison between site and study teams
• •Proven performance in earlier role
• •Licensure, Registration and/or Certification Required by Law:
• •Licensure, Registration and/or Certification Required by SJCRH Only:
• •6 more items(s)

Responsibilities

• •The Clinical Research Associate I or II is responsible for performing data abstraction, collection, and entry to support clinical research
• •Provides data and reports to the collaborating research organization or study sponsor
• •Assist clinical research study team(s) in general administrative activities under guidance
• •Maintain sufficient inventory of material, supplies, and equipment for performance of clinical research-related activities
• •test samples, regulatory documents, etc.)
• •Participate in data retrieval, reporting, and preparation of files for various studies
• •Executes routine tasks under guidance and/ or supervision
• •Shows attention to detail, produces quality work on time
• •Applies basic knowledge of clinical study support processes in delivery of routine tasks (e.g., administrative activities, documentation, inventory maintenance) with guidance
• •Act as site study coordinator conducting informed consent process as designated, and assisting with protocol submissions (internally sponsored and/or externally sponsored) for review by federal or institutional committees (e.g. investigator files, case report forms, study data)
• •Perform data abstraction, collection, and entry to support clinical research
• •Prepare detailed data reports as required
• •(assistance in clinical procedures; medication instruction, monitoring, and documentation; Minimum Education and/or Training:
• •Understands the task at hand, seeks out information, and draws conclusions from available data to deliver outcomes
• •Contributes to study management and research procedures by consistently executing on assigned tasks in compliance with GCP guidelines, with minimal supervision
• •Applies understanding of clinical study/site operations to address requirements (e.g., study selection and set-up, clinical monitoring, risk mitigation support)
• •S. state and municipal pay transparency laws, St
• •14 more items(s)