Quality Assurance Professional for Clinical Trials
Clients in the pharmaceutical industry require professionals to ensure the highest quality standards are met throughout clinical trials. In this role, you will contribute to the development of procedures and tools that maintain quality management systems.
Responsibilities include reviewing and approving quality system documents, recommending new or revised documents where necessary, advising on training needs, and providing consultation on regulatory compliance. This includes documenting events, escalating concerns, and completing root cause analyses and corrective actions.
A Bachelor's degree in a related field or equivalent experience is required, along with demonstrated ability to apply quality systems within a regulated environment. Experience in quality control/quality assurance roles and functional areas such as medical writing, regulatory affairs, or clinical trial management is highly valued. Effective communication, project management, and interpersonal skills are essential.