Senior Clinical Data Analyst - Regulatory Submissions - Guarulhos - beBeeDataStandardizer

The EHS Manager provides strategic and technical leadership to ensure best-in-class Environment, Health, and Safety (EHS) performance across H.B. Fuller's Latin American business and facilities. · Identify and translate EHS requirements from applicable regulations for facilities ...

We're building a world of health around every consumer and surrounding ourselves with dedicated colleagues who are passionate about transforming healthcare. · We reach millions of Americans through our local presence, digital channels and more than 300,000 purpose-driven colleagu ...

We are seeking a Manager to lead our Cyber Resiliency efforts for CVS Health's Digital, Data, Analytics & Technology (DDAT) Cybersecurity GRC team. The successful candidate will have experience in cyber resiliency related activities and be able to execute on strategic direction. ...

Conexión con profesionales innovadores para hacer crecer tu carrera. · ...

The Director of Regulatory Affairs is responsible for developing regulatory strategies and providing guidance to product development and commercial teams in support our products Portfolio. · ...

We are seeking an experienced · Regulatory Affairs Lead to drive regulatory strategy and execution for the Brazilian market.This role will lead end-to-end regulatory planning, · stakeholder engagement,and submission managementto support product registration,lifecycle maintenance ...

The Senior Analyst, Regulatory Affairs (P6) provides support to the C-ROSS(MS) Product Leader (CRPL) and Regulatory Regional Leader (RRL) for regulatory activities for products in the assigned portfolio. · Mandatory Requirements Fluent english (writting and verbal) · ...

Prepares and coordinates regulatory submissions to EU CTIS and other applications. · Provides local regulatory strategy advice to internal clients. · Coordinates with internal departments to ensure site start-up activities align with submission activities. · ...

We are seeking a Regulatory Submissions Coordinator to support our team in Brasil. · ...

The Regional Director will manage the Regional CMC team ensuring seamless integration between global Regulatory CMC strategies and local affiliate execution. · ...

The Regulatory Affairs Analyst will be responsible for managing regulatory submissions and ensuring compliance with local and international regulatory requirements. · This role plays a key part in supporting new product registrations, post-marketing activities, and regulatory str ...

As a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you will be central to the successful delivery of complex global oncology clinical trials for some of the world's most renowned pharmaceutical companies. · ...

As a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you will be central to the successful delivery of complex global oncology clinical trials (Phases I–III) for some of the world's most renowned and innovative pharmaceutical ...

Key Responsibilities · Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing. · Draft, review, and quality-check clinical trial regulatory core study documentation at global and country level . · Engage directl ...

This is a great opportunity for you to further develop your skills and become an expert in clinical research. · As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the h ...

We are searching for the best talent for a Oncology Regulatory Affairs Manager position, based in São Paulo, Bogotá or Mexico City. · We are looking for a talented professional to join our team as an Oncology Regulatory Affairs Manager. The successful candidate will be responsibl ...

Manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · ...

· Work closely with Project Manager (PM) to define regulatory / importation strategies for the assigned studies · ...

We believe health is everything. · Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented treated and cured where treatments are smarter and less invasive and solutions are personal. · ...

PharmEng Technology is seeking a highly motivated and experienced Analista de Assuntos Regulatórios to join our team in São Paulo Brazil. · ...

We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · ...