Country Regulatory Submissions Specialist

A global contract research organization is seeking a Country Approval Specialist to manage regulatory submissions and activate investigative sites. The candidate will provide advice on regulatory strategies and coordinate with internal teams to ensure timely site activation. A Bachelor’s degree and a minimum of 2 years of relevant experience are required....

A leading global contract research organization is seeking a Country Approval Specialist in Buenos Aires, Argentina. In this role, you will be responsible for coordinating regulatory country submissions for site activation, providing strategic advice to internal clients, and ensuring compliance with local regulations. Candidates must possess a Bachelor’s...

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....

Country Approval Specialist Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, who powers our PPD® clinical research portfolio,...

**Description - External** - We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost...

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. Distribute reports/data to internal and external third...

Country Approval Specialist – PPD PPD is a leading global contract research organization. At PPD we are passionate, deliberate, and driven by our purpose — to improve health. Site and Patient Access is a global department working to provide rapid site activation and patient access to our clients. Our innovative approach is designed to help save our...

JOB DESCRIPTION External - We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve...

Description - External - We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD – thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve...

Regulatory Affairs Sr Specialist - LATAM Johnson & Johnson 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 than 1...