Regulatory Publishing Specialist

A global biopharmaceutical solutions organization seeks a Regulatory Publishing Specialist with Veeva experience in Buenos Aires. This mid-level role includes assembler tasks, document publishing, and ensuring compliance with submission standards. Candidates should have strong skills in publishing systems and document quality control. The company values...

Regulatory Publishing Specialist- Veeva Experience Required Description Regulatory Publishing Specialist- Veeva Experience Required Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. Our Clinical Development model brings the customer and the patient to the center of everything we do....

Regulatory Publishing Specialist - Veeva Experience Required Syneos - Clinical and Corporate - Prod Regulatory Publishing Specialist - Veeva Experience Required Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into...

**Join Our Team as a Freelance Desktop Publishing (DTP) Specialist in Latin America!** **Company**: Effectiff **Position**: Freelance Desktop Publishing (DTP) Specialist **Location**: Latin America (Remote) **About Us**: Effectiff is a dynamic language service provider committed to delivering top-quality translation and localization solutions. We're...

**Description** Regulatory Publishing Specialist - Veeva Experience Required Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model...

Regulatory Affairs Specialist – Regulatory Affairs / Southern Cone At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity.Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more...

Job Overview Essential Functions - Acts as a Regulatory Team Leader on more complex projects, which may include technical writing; - Prepares and/or reviews regulatory documentation in area of expertise, as appropriate; - Establishes relationships with many customers; may meet face to face without rest of the team to discuss regulatory issues, present...

Overview At Cognizant, we have an ideal opportunity for you to be part of one of the largest companies in the digital industry worldwide. We look for people who contribute new ideas, thriving in a dynamic and growing environment. We promote an inclusive culture where we value different perspectives. We are looking for a Webinar Publishing Specialist to work...

Regulatory Submissions Specialist (with Portuguese) IQVIA This role will require special working days as National Holidays and weekends. Job Overview As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities. Review, assess, and process safety data and information received from various sources....

Careers that Change Lives In this exciting role as a Regulatory Affairs Specialist, you will lead and prepare Regulatory Affairs (RA) meetings (regulatory status) involving cross‑functional business partners under your responsibility. You will provide status on time about projects and all applicable regulatory activities assigned per Senior Supervisor or...