ID号码 0000053749: Clinical Research Coordinator (CRC) with TÜV Rheinland Certified Qualification

此ID页面可选择下列语言: German
认证项目名称:Clinical Research Coordinator (CRC) with TÜV Rheinland Certified Qualification
入学要求:

Additional qualification for specialist medical personnel (e.g. Nurses / Doctor’s Assistants, Medical Documentation Personnel, Specialized Medical Employees, Medical Technical Assistants).

Successful participation in the qualification “Clinical Research Coordinator (CRC) with TÜV Rheinland Certified Qualification“ according to the PAREXEL International training concept, comprising 40 teaching units, recognized by the personnel certification body. Admission to the exam is granted with 80% attendance of the training course.

考试内容:
  • Written Examination (Multiple Choice)
必需具备的能力:

During the examination participants prove their knowledge in the following areas:

  • Fundamentals of clinical research
  • Guidelines and legal fundamentals
  • Responsibilities ICH-GCP
  • Essential documents
  • Monitoring clinical trials
  • Requirements for source data
  • AE / SAE security data
  • Dealing with Test medication
  • Trial coordination
  • Quality Assurance

Successful participants are qualified in the independent and responsible organization and implementation of clinical trials. They have a good understanding of the legal framework and ethical fundamentals of  “Good Clinical Practice” (GCP), which regulate the implementation of medical trials today. They play a central role as contact person for test doctors, monitors, the trial coordination office, and patients alike. They make an essential contribution towards looking after the trial participants, the collection and documentation of trial relevant data and the preparation and accompaniment of monitor visits (rounds), audits and inspections.

合作伙伴:https://www.clinical-research-training.com/poland/en/clinical-research-coordinator-program
目前适用地区:德国