Regulatory Specialist

Regulatory Affairs Specialist (Spain) Company: Indero (formerly Innovaderm) Indero, a Contract Research Organization (CRO) specializing in dermatology and rheumatology, is expanding globally and seeks a Regulatory Affairs Specialist for Spain. Responsibilities Preparation of regulatory documents, CTA packages, and submissions in assigned countries to ensure...

A pharmaceutical company located in Madrid is seeking a Regulatory Affairs Specialist. This role involves managing global regulatory submissions, ensuring compliance with regulations, and collaborating with cross-functional teams. The ideal candidate will have at least 3 years of experience in regulatory roles within the pharmaceutical industry, a strong...

The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions. This role will be responsible for sponsor-facing regulatory leadership and management of regulatory deliverables...

IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human ingenuity to drive healthcare forward....

A leading healthcare data company is seeking a Regulatory Affairs Specialist to support post-approval regulatory activities for human medicinal products in Spain. This role requires at least 4 years of experience in regulatory affairs and proficiency in English and Spanish. Responsibilities include preparing regulatory documents, ensuring compliance with...

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis. We are looking for someone who can autonomously carry on the work within the scope of their activities and interacts with the Direct Manager to define priorities and manages workload....

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis.¿Todo listo para enviar su solicitud? Asegúrese de comprender todas las responsabilidades y tareas asociadas a este puesto antes de continuar.We are looking for someone who can...

The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions.This role will be responsible for sponsor-facing regulatory leadership and management of regulatory deliverables...

OverviewInscríbase rápido, consulte la descripción completa desplazándose hacia abajo para conocer todos los requisitos de este puesto.Due to ongoing global expansion, Indero is looking to hire a Regulatory Affairs Specialist. In this position, you will be responsible for preparation and submission of part I and / or part II following EU CTR and other...

Overview Due to ongoing global expansion, Indero is looking to hire a Regulatory Affairs Specialist. In this position, you will be responsible for preparation and submission of part I and / or part II following EU CTR and other applications created within or outside of the company to ensure documentation comply with applicable regulations and guidelines and...