Title: Clinical QA Training Specialist
Location: 8368 Clayton Boulevard Clayton NC 27520
Job Description: - Responsible for maintaining and developing training profiles and documentation for Clinical QA and MD/EG departments.
- Maintain information/documents related to training within Clinical QA and MD/EG departments including training matrices.
- Monitor and report the status of training requirement completions.
- Maintain position-specific training curricula for job functions in the Clinical and Clinical QA departments.
- Knowledge Skills and Abilities:
- Excellent Knowledge and understanding of quality and regulatory requirements for the biotechnology and pharmaceutical industry.
- Good familiarity with quality systems and compliant maintenance of quality-related documentation and records including knowledge of electronic document control systems.
- Proficient in word processing and spreadsheet applications.
- Proven ability to prioritize competing tasks and meet deadlines to ensure compliance. Excellent oral and written communication skills and the ability to work in a cross-functional and multi-cultural team environment.
Education:
- Bachelors degree in a scientific or related field.
Experience: - Typically requires a minimum of 6 years of relevant experience with document systems within a Quality Organization or related area in the Biologics Biotech or Pharmaceutical industry.
Title: Clinical QA Training Specialist Location: 8368 Clayton Boulevard Clayton NC 27520 Job Description: Responsible for maintaining and developing training profiles and documentation for Clinical QA and MD/EG departments. Maintain information/documents related to training within Clinical Q...
Title: Clinical QA Training Specialist
Location: 8368 Clayton Boulevard Clayton NC 27520
Job Description: - Responsible for maintaining and developing training profiles and documentation for Clinical QA and MD/EG departments.
- Maintain information/documents related to training within Clinical QA and MD/EG departments including training matrices.
- Monitor and report the status of training requirement completions.
- Maintain position-specific training curricula for job functions in the Clinical and Clinical QA departments.
- Knowledge Skills and Abilities:
- Excellent Knowledge and understanding of quality and regulatory requirements for the biotechnology and pharmaceutical industry.
- Good familiarity with quality systems and compliant maintenance of quality-related documentation and records including knowledge of electronic document control systems.
- Proficient in word processing and spreadsheet applications.
- Proven ability to prioritize competing tasks and meet deadlines to ensure compliance. Excellent oral and written communication skills and the ability to work in a cross-functional and multi-cultural team environment.
Education:
- Bachelors degree in a scientific or related field.
Experience: - Typically requires a minimum of 6 years of relevant experience with document systems within a Quality Organization or related area in the Biologics Biotech or Pharmaceutical industry.
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