What are the responsibilities and job description for the Clinical QA Document Specialist position at The Fountain Group?
Currently I have an opening for a Clinical QA Document Specialist located in Clayton, NC. Details for the position are as follows:
Job Description:
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 status of training requirement completions.
- Maintain position-specific training curricula for job functions in the Clinical and Clinical QA departments.
- 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.
- Bachelor’s degree required with quality/documentation experience within the biotech/pharma industry. Experienced in managing and updating documents in relation to training documents (clinical, manufacturing, engineering, etc.).
- Quality Systems Experience - EDMS, QDMS, QMS, etc.
- 6-month contract, with potential for extension/conversion
- Pay: $25-28.50 hourly, depending on experience level
- Full onsite position, M-F, 9am-5pm
Salary : $25 - $29
