The regulatory function is vital in making safe and effective healthcare products available worldwide. Individuals who ensure regulatory compliance and prepare submissions, as well as those whose main job function is clinical affairs or quality assurance are all considered regulatory professionals.
One of our most valuable contributions to the profession is the Regulatory Code of Ethics. The Code of Ethics provides regulatory professionals with core values that hold them to the highest standards of professional conduct.
Like all professions, regulatory is based on a shared set of competencies. The Regulatory Competency Framework describes the essential elements of what is required of regulatory professionals at four major career and professional levels.
Join the brightest minds in regulatory at the annual Regulatory Convergence. See the global regulatory community in action. Intensive workshops. Topical sessions. Meet ups with regulators. This is where it all comes together.
Under the direction of the Department Vice Chair and the Clinical Trials Manager, the Study Coordinator is responsible for the coordination of clinical tasks and conduct of administrative tasks required to successfully conduct clinical trials within the Department of Radiation Oncology. Responsibilities include preparing and updating study orders based on an in-depth analysis of the protocol; planning and coordinating logistics and scheduling study visits with nursing and other clinical staff within the Department and extra-departmentally; identifying potential study subjects for recruitment; regular communication with and reporting to investigators, sponsors, monitors and subjecgts; reporting/recording serious adverse events and deviations to compliance committees; providing administrative, regulatory and data management support as needed. Exercise critical thinking and implement a dynamic, continuous and solution-oriented approach in the coordination of clinical trials.
Bacherlor's degree strong preferred;
3 years or more experience in FDA governed trials strongly preferred;
3+ years in complex oncology trials strongly preferred.
Self-directed and proactive
Critical thinking skills to be able to implement a dynamic, continuous and solution-oriented approach in the coordination of clinical trials
Ability to determine the most appropriate and efficient method of completing each project
UCLA is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected Veteran status.
Altria Group is a FORTUNE 200 company that leads the premier tobacco companies in the United States. Headquartered in Richmond, Virginia, Altria Group holds diversified positions across tobacco, alcohol, and cannabis. Our tobacco companies include some of the most enduring names in American business: Philip Morris USA, U.S. Smokeless Tobacco Company, John Middleton. We have 35 percent ownership of JUUL Labs, Inc., the nation’s leading e-vapor company. And we have an 80 percent interest in Helix Innovations, which manufactures and markets on!, an oral tobacco-derived nicotine pouch product. We complement our total tobacco business with our ownership of Ste. Michelle Wine Estates and our significant equity investment in Anheuser-Busch InBev, the world's largest brewer. Altria’s significant stake in Cronos Group, a leading global cannabinoid company, represents an exciting new global growth opportunity.
At Altria, we celebrate the power of diverse teams working together to shape our future. We are inspired to bring our best because our unique strengths are valued. We believe our personal success and progress should be guided by Our Cultural Aspiration, a new articulation of what w...e value and who we aspire to be, collectively. Our Cultural Aspiration respects and complements individual identity, embracing each other’s unique strengths, welcoming newcomers and developing the best, most inclusive and diverse teams. Over the next 10 years, we have the opportunity to make more progress on harm reduction than we have in the past 50 years. Join us as we work together to shape a better future for adult tobacco consumers, our employees, and our shareholders. Each Altria company is an equal opportunity employer.