Regulatory Affairs Specialist

hace 1 semana

Madrid Centro, Madrid, España Sin nombre A tiempo completo

**About Sin nombre**

Sin nombre is a leading Contract Research Organization (CRO) that provides high-quality services to the pharmaceutical and biotechnology industries. We are committed to delivering innovative solutions that meet the evolving needs of our clients.

**Job Summary**

We are seeking a highly skilled Regulatory Submissions Coordinator to join our team in Madrid. As a key member of our regulatory affairs department, you will be responsible for ensuring the timely and accurate submission of regulatory documents to various authorities.

**Key Responsibilities**

  • Provide insightful input on regulatory submissions documents and timelines;
  • Ensure submissions comply with applicable regulations and guidance documents;
  • Advise on changing country regulations and compliance requirements;
  • Track submissions and ensure timely filing of documents.

**Requirements**

  • At least 1 year of experience within regulatory affairs in clinical research;
  • Hands-on experience preparing, reviewing, and submitting regulatory documentation;
  • Fluent in English and Spanish.

**What We Offer**

  • Permanent position with a flexible start date;
  • Great training and onboarding program;
  • 4 opportunities of promotion per year.

**About Us**

Sin nombre is a dynamic and growing company that values innovation, teamwork, and customer satisfaction. We are committed to providing a positive and inclusive work environment that supports the growth and development of our employees.

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