Regulatory & Clinical Affairs Associate

Description The Regulatory Affairs Strategist delivers innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities. The RA Strategist is responsible for regulatory aspects related to clinical trial regulatory submissions in alignment with the global business strategy and in partnership with the...

The Manager, Regulatory Affairs is responsible to ensure the services provided by the regional regulatory affairs department are conducted according to Innovaderm’s standard operating procedures, applicable regulations and good clinical practices and to the Sponsor’s satisfaction. Responsibilities include providing leadership on regulatory activities...

**Scope**: A fantastic opportunity has presented itself to join a globally renowned ‘pure play’ Aesthetic Company. Due to the rapid growth of this business, our client are seeking a high calibre Regulatory Affairs Director to join their team in Barcelona. This establishment has a portfolio of differentiated, complementary aesthetic technologies with a...

**Scope**: Director of regulatory affairs position that has been opened to further accompany the growth of the company on this sector. Although our client is a historically pharma oriented manufacturer, they have in the recent years expanded their activities in the Medical Aesthetics area, with products currently on market in the Dermal and Hyaluronic acid...

Actualizado 10/04/2024 Formación en Ciencias de la Salud Master en Regulatory Affairs o prácticas en Regualtory Affairs¿Dónde vas a trabajar?Importante compañía con sede en Vallés Occidental, centrada en el desarrollo y la fabricación de productos sanitarios y complementos alimenticios innovadores¿Qué harás en tu nuevo puesto?Técnico/a para la...

The Aixial Group is seeking a Sr. Regulatory Lead for this client dedicated opportunity with 8 years of experience in Regulatory Affairs. Remote based in Spain or Portugal. Contribute to the development of the regulatory strategy for the respective portfolio, working collaboratively with the global regulatory office community and cross functional teams to...

Job Overview: As a Senior CRA specializing in ophthalmology, you will play a crucial role in the planning, implementation, monitoring, and management of clinical trials related to ophthalmic drugs, devices, or therapies. You will ensure that clinical trials are conducted in accordance with applicable regulatory requirements, protocols, and standard operating...

Desde el departamento de Pharma de Antal International nos encontramos en búsqueda de un Senior Regulatory Affairs para trabajar en una importane multinacional Dermocosmética para la parte de regulación de medicamentos ubicada en Barcelona. Formación Universitaria en Ciencias de la SaludMás de 4 años con posiciones de Regulatory Affairs en Industria...

Robert Walters is hiring a Regulatory Affairs Manager in Barcelona. Our client is an important pharmaceutical company specialized in medical nutrition. As a Regulatory Affairs Manager, the candidate reports to the Director of RD&A.Its objective is to ensure regulatory compliance of the product portfolio (marketed and investigational products) in all the...

Robert Walters is hiring a Regulatory Affairs Manager in Barcelona.Our client is an important pharmaceutical company specialized in medical nutrition.As a Regulatory Affairs Manager, the candidate reports to the Director of RD&A.Its objective is to ensure regulatory compliance of the product portfolio (marketed and investigational products) in all the...

For more than 75 years, Grifols has worked to improve the health and well-being of people around the world. We are a global healthcare company that produces essential plasma-derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services they need to deliver expert medical care. Headquartered in...

Técnico/a para la preparación de la documentación regulatoria de los productos desarrollados por la empresa, complementos alimenticios, productos sanitarios clase IIa, productos sanitarios in vitro y cosméticos. * Formación en Ciencias de la Salud: Farmacia, biología, bioquímica, o similar * Master en Regulatory Affairs * Persona responsable,...

Farmaprojects, part of Polpharma Group B.V., is a B2B Pharmaceutical Laboratory company offering a broad Portfolio of Generic Pharmaceutical Products and Value Added Medicines. For our office in Barcelona, Farmaprojects is looking for a new Senior Regulatory Affairs Specialist to join our Regulatory Affairs Department. At Farmaprojects, you can expect: To be...

Farmaprojects, part of Polpharma Group B.V., is a B2B Pharmaceutical Laboratory company offering a broad Portfolio of Generic Pharmaceutical Products and Value Added Medicines. For our office in Barcelona, Farmaprojects is looking for a new Senior Regulatory Affairs Specialist to join our Regulatory Affairs Department. At Farmaprojects, you can expect: To be...

The Opportunity The Regulatory Affairs Graduate is responsible for formatting, assembling, and timely preparation of documents for domestic and international regulatory submissions and ensuring cosmetic product compliance with applicable regulations.  He/She supports the regulatory team in ensuring compliance of finished cosmetic products, including...

The OpportunityThe Regulatory Affairs Graduate is responsible for formatting, assembling, and timely preparation of documents for domestic and international regulatory submissions and ensuring cosmetic product compliance with applicable regulations. He/She supports the regulatory team in ensuring compliance of finished cosmetic products, including...

Técnico/a para la preparación de la documentación regulatoria de los productos desarrollados por la empresa, complementos alimenticios, productos sanitarios clase IIa, productos sanitarios in vitro y cosméticos. Fabricante de productos sanitarios y complementos alimenticios|Formación en Ciencias de la Salud - Formación en Ciencias de la Salud: Grado...

Contract: Permanent Career Opportunity Closing Date: 10/02/23 **The Role**: - The preparation of CMC regulatory documents and/or other regulatory documents for MAA and Post Approval Lifecycle projects including renewals, variations, annual reports etc. - Working with manufacturing sites on change control projects; providing regulatory advice and strategic...

**¿Quieres formar parte de nuestro equipo de **Regulatory Affairs**? Si tienes....**: Interés en Regulatory Affairs del sector Consumer Healthcare y eres **Tus Retos**: Tu **Misión **es controlar el cumplimiento con la legislación de los productos asignados, de acuerdo con las directrices del Responsable de Registros y el marco legal vigente, con el fin...

**Description** **Clinical Trial Manager** 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 brings the customer and the patient to...