Global Regulatory Submissions Specialist

A leading pharmaceutical company in Madrid is looking for a Regulatory Affairs Specialist to support global regulatory submissions and ensure compliance with regulatory requirements. The role involves preparing regulatory dossiers, collaborating with cross-functional teams, and maintaining high-quality regulatory documentation. This position requires a...

A leading international CRO is searching for a Regulatory Submissions Specialist to join their regulatory team. This position is remote, allowing flexibility. The ideal candidate will be fluent in English and have strong planning, problem-solving, and organizational skills. The role involves managing regulatory requirements, ensuring compliance, and...

A leading global CRO is seeking a Regulatory Submissions Specialist to join their team in a remote capacity. This role involves developing knowledge of regulatory requirements, managing contracts and budgets, and ensuring quality standards are met. Candidates should be fluent in English and possess strong planning, problem-solving, and organizational skills....

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.The Regulatory Submissions Specialist contributes to the management and development of procedures related to the activities in which he / she is involved in and ensures that the...

A global CRO is looking for a Regulatory Submissions Specialist to join their regulatory team remotely. The ideal candidate will manage regulatory submission activities, ensuring compliance with global and local requirements. The role demands fluency in English and strong planning and organizational skills. Experience in contract negotiation and procedural...

A pharmaceutical company in Madrid is seeking a Regulatory Affairs professional. The role involves managing regulatory submissions and ensuring compliance with pharmaceutical regulations. Key responsibilities include preparing and submitting regulatory dossiers, supporting product registrations, and collaborating with cross-functional teams. The ideal...

A global leader in clinical research and healthcare intelligence is seeking a Senior Translation Project Manager for Regulatory Submissions in Madrid. You will manage multiple translation projects, ensuring high-quality standards and maintaining client relationships. Ideal candidates have over 4 years of experience in project management, particularly with...

A clinical research organization in Madrid is seeking a Regulatory Specialist to ensure site activation readiness for clinical trials. The ideal candidate will have at least one year of relevant experience and a bachelor's degree in life sciences or similar. Responsibilities include preparing regulatory submissions and maintaining site-level project plans,...

Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Graduate to join our Clinical Operations team as a Entry Level Regulatory Submissions Coordinator. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your...

A contract research organization is seeking a Senior Regulatory Affairs Specialist in Madrid to lead regulatory activities for clinical trials. This role involves overseeing complex global submissions, providing expertise to project teams, and mentoring junior colleagues. The ideal candidate has a Bachelor's degree, 3-5 years of regulatory experience, and a...