Regulatory Affairs Job Positions in Brazil - 74 Positions AvailableWhen our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health.
From clinical trials to regulatory, consulting, and market access, every clinical aspect is vital.Job Purpose/ Summary: Responsible for overall global strategies and operational aspects of Regulatory Affairs Study Start-up (RASSU) department at CTI.
Provides leadership and direction to all members of global RASSU, ensuring timelines, budget, and quality measures are met.Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services.
Role will include management of clinical trial applications to Competent Authorities, Ethics Committees, and Regulatory Agencies, and the research, review, and reporting on applicable global regulations.Carrying out, controlling, and implementing activities related to the company's quality system.
Carrying out, controlling, and implementing the regulatory processes applicable to the company's activities and products.
Providing support to the LATAM RAQA manager in the department.Essential Functions: Coordinates timely collection and management of data, metrics, experience statements for proposal and budget development in response to Request for Proposals (RFPs).Patients are at the heart of everything we do.
As part of our Medical Affairs team, you'll foster internal and external collaboration to generate and disseminate evidence-based clinical practices to help impact patient lives and advance the field.Are you interested in a leadership opportunity to drive the implementation of effective Clinical Onco-hematology strategies for a multi-national pharmaceutical company?
If so, this role may be for you!
As Medical Affairs Onco-Hematology Director, you will be responsible for leading initiatives in this area.Job Summary: In the Global Regulatory Affairs (GRA) team, we have an opening for a Regulatory Manager for the Latin America (LATAM) region to coordinate and drive regulatory and advocacy activities for our Bioactives (biotechnology food, feed, and technical products).Vice President for Clinical, Medical & Regulatory LATAM São Paulo, Brazil.
Are you ready for a life-changing career at Novo Nordisk?
Working at Novo Nordisk is never just a job; it is an opportunity to have a significant impact.The Regulatory Risk Officer is a strategic professional who stays abreast of developments within their field and contributes to directional strategy by considering their application in their job and the business.
Recognized technical authority for an area.Sr Regulatory Affairs Specialist: Provides regulatory advice and carries out projects in the provision of regulatory affairs services.
Acts as liaison with internal team members in the provision of these services.
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