Eurofins Scientific is a global leader in bioanalytical testing, providing a comprehensive range of laboratory services across the food, environmental, pharmaceutical, and cosmetic industries. With a network of over 900 laboratories and approximately 61,000 employees worldwide, the company is a critical player in ensuring the safety and quality of products and services through advanced scientific analysis.

In Spain, Eurofins maintains a robust presence with numerous specialized laboratories and administrative hubs across the country. The company offers diverse career paths for international professionals, ranging from highly specialized scientific roles in chromatography and microbiology to corporate functions in IT, finance, and project management. Their multicultural environment and the frequent requirement for multilingual staff in many departments make it an attractive destination for international talent.

Eurofins was founded in 1987 in Nantes, France, starting with just 10 employees to market a patented technology used to verify the origin and purity of food and beverages. Since then, it has grown through aggressive acquisition and organic growth into a global scientific services giant.

For international professionals

Offers a wide variety of roles for English speakers, particularly in IT, service desk, and corporate functions.
Maintains a decentralized network of laboratories across Spain, providing job opportunities in multiple regions beyond just Madrid and Barcelona.
As a global leader in the TIC (Testing, Inspection, and Certification) sector, it provides a stable environment for scientific professionals.
Frequently hires for 'Multilingual Service Desk' and 'IT Business Analyst' roles which are well-suited for international profiles.

Ophthalmologist, Cosmetic Clinical Study Supervision

Eurofins

This job was originally posted in Spanish and automatically translated to English. You'll most likely need Spanish to apply.

Job Description

Company Description

Multinational Services company dedicated to the Cosmetic sector requires the collaboration of an ophthalmologist for clinical studies under medical control.

Job Description

Execution of clinical studies from start to finish, completing all necessary documentation and following good clinical practices.
Monitoring of subjects in specific clinical studies that require their presence for assessment or potential side effects.
Interpretation of results in the Case Report Forms.
Collaboration in the creation, drafting, and adaptation of clinical study protocols.
Drafting of the discussion and conclusion of final reports.
Review of said reports in order to provide improvements and complete any data deemed necessary.
Reading of clinical study protocols (general and specific) and associated documentation.
Occasional assistance with queries regarding future studies (preferably via email consultations).

Requirements

Ophthalmology (Specialty in the process of recognition/homologation in Spain is acceptable)

Must be registered as self-employed (autónomo)

Required documentation: AEAT Certificate - Social Security Certificate

Additional Information

Part-time:

Collaborations may arise depending on the duration of the study performed.

Commercial contract offered (self-employed)

Hourly rate to be agreed upon

View original advert (Spanish)

Descripción de la empresa

Empresa Multinacional de Servicios dedicada al sector Cosmético precisa colaborar con un/a oftalmólogo/a para estudios clínicos bajo control médico.

Descripción del empleo

Ejecución de los estudios clínicos desde el principio hasta el fin, completando toda la documentación necesaria y siguiendo las buenas prácticas clínicas.
Control de sujetos en estudios clínicos puntuales que requieran su presencia por su valoración o sus posibles efectos secundarios.
Interpretación de resultados en los Cuadernos de Recogida de Datos.
Colaboración en la creación, redacción y adaptación de protocolos de estudios clínicos.
Redacción de la discusión y conclusión de los informes finales.
Revisión de dichos informes con objeto de aportar mejoras y completar los datos que se estimen necesarios.
Lectura de protocolos de estudios clínicos (generales y específicos) y documentación asociada.
Asistencia puntual a dudas sobre futuros estudios (preferiblemente consultas vía e-mail),