US: Clinical Research Quality Assurance
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Oct 30, 2012, 6:41:14 PM10/30/12
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US: Clinical Research Quality Assurance
To apply for this position, please visit this Website.
http://biotech.fyicenter.com/jobs/99889453_Clinical_Research_Quality_Assurance.html
Date: 30-Oct-2012
To see other BioTech job opportunities, please visit http://biotech.fyicenter.com/
Clinical Research Quality Assurance
* Personal qualities and interpersonal communication skills to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public under all circumstances * Effectively communicate both orally and in writing. Able to effectively present information.
* Demonstrates leadership ability, accepts responsibility, exercises authority, and functions independently using effective written and verbal communications * Detail oriented and teamwork skills * Motivated, organized, able to perform multiple tasks in a timely manner, and work efficiently under pressure. Ability to self-monitor progress and complete assigned tasks independently. * Ability to manage multiple duties and function independently * Critical thinker with perceptual and analytical approach to problem solving * Able to perform diverse clerical duties * Working knowledge of Microsoft Office applications of Word, Excel, PowerPoint, Outlook, and Internet knowledge skills * Knowledge of audit processes and monitoring procedures (preferred) * Minimum 1- 5 years clinical research experience * Bachelor's degree in nursing or health related field (non-nursing applicants) * Minimum 3-5 years clinical trials monitoring/auditing in a pharmaceutical company or CRO (preferred) * Master Degree in health related field (preferred)
. * Reviews quality assurance standards, studies existing policies and procedures, and interviews personnel and customers (industry representatives) to evaluate effectiveness of quality assurance program.
* Writes/revises departmental quality assurance SOPs as required.
* Conducts ongoing review of clinical trial patient research charts and data reporting for compliance with federal regulation, institutional policy and study specific requirements. * Selects specific trial or study staff for data review. Validates source data and accuracy in reporting.
Thank you,
BioTech FYI Center
http://biotech.fyicenter.com/
To apply for this position, please visit this Website.
http://biotech.fyicenter.com/jobs/99889453_Clinical_Research_Quality_Assurance.html
Date: 30-Oct-2012
To see other BioTech job opportunities, please visit http://biotech.fyicenter.com/
Clinical Research Quality Assurance
* Personal qualities and interpersonal communication skills to interact and maintain good relationships with a broad spectrum of healthcare disciplines and the public under all circumstances * Effectively communicate both orally and in writing. Able to effectively present information.
* Demonstrates leadership ability, accepts responsibility, exercises authority, and functions independently using effective written and verbal communications * Detail oriented and teamwork skills * Motivated, organized, able to perform multiple tasks in a timely manner, and work efficiently under pressure. Ability to self-monitor progress and complete assigned tasks independently. * Ability to manage multiple duties and function independently * Critical thinker with perceptual and analytical approach to problem solving * Able to perform diverse clerical duties * Working knowledge of Microsoft Office applications of Word, Excel, PowerPoint, Outlook, and Internet knowledge skills * Knowledge of audit processes and monitoring procedures (preferred) * Minimum 1- 5 years clinical research experience * Bachelor's degree in nursing or health related field (non-nursing applicants) * Minimum 3-5 years clinical trials monitoring/auditing in a pharmaceutical company or CRO (preferred) * Master Degree in health related field (preferred)
. * Reviews quality assurance standards, studies existing policies and procedures, and interviews personnel and customers (industry representatives) to evaluate effectiveness of quality assurance program.
* Writes/revises departmental quality assurance SOPs as required.
* Conducts ongoing review of clinical trial patient research charts and data reporting for compliance with federal regulation, institutional policy and study specific requirements. * Selects specific trial or study staff for data review. Validates source data and accuracy in reporting.
Thank you,
BioTech FYI Center
http://biotech.fyicenter.com/
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