Overview:
Lead and perform Clinical Quality Assurance (QA) initiatives and duties at PharPoint Research, including all project and non-project activities performed. Responsible for assisting with the creation and implementation of quality initiatives at the company, including but not limited to: Standard Operating Procedures (SOPs) and training, computer systems validation (CSV), and Quality Management System (QMS).
What you will do:
The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.
Qualifications:
Employer Statement
We’re in the business of helping clients improve global health. We’re proud to offer more than just a stable paycheck - we foster an environment of understanding, and value a better work-life balance. Here, your voice matters. Our teammates are innovative, industry-leading professionals and experts in their fields. Together, we do big things. Join us today as we work together towards a healthier tomorrow.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.
PharPoint is unable to sponsor work visas at this time
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