Graduate Strategy Consultant

MMS; Madrid; A distancia; EUR 70.000 - 100.000; Jornada completa

Descripción de la vacante

A leading data-focused clinical research organization is seeking a Principal Regulatory Strategist for Europe. This consultancy role involves providing expert guidance on regulatory matters, conducting technical reviews, and influencing policy recommendations in the pharmaceutical industry. The ideal candidate has advanced qualifications and a solid reputation within the field, and will thrive in a remote-based setting.

Formación

• Emerging leader with sustained performance and accomplishments.
• Basics of CRO operations and drug development.
• Ability to provide recommendations on regulatory changes.

Responsabilidades

• Provide consulting and advisory services on regulatory issues.
• Conduct senior technical reviews for complex projects.
• Participate in project teams and identify updated policies.

Conocimientos

Proficiency with MS Office applications

Complex regulatory issues consultation

Technical reviews for regulatory projects

Educación

College degree in Biological Science

Masters or PhD preferred

Descripción del empleo

Principal Regulatory Strategist (CRO / Pharma Industry) - Europe

Job Overview

MMS is an award-winning, data-focused clinical research organization (CRO) supporting the pharmaceutical, biotech, and medical device industries. We excel in complex trial data management and regulatory submissions, with a global presence across four continents. Our commitment to customer satisfaction and fostering an inclusive, collaborative work environment makes MMS a great place to thrive. Join us and be part of shaping the future of clinical research.

This is a full-time consultancy role, remote-based.

Responsibilities

1. Provide consulting and advisory services on complex regulatory issues or projects.
2. Conduct senior technical reviews for complex regulatory projects.
3. Participate in project teams, offering expertise on regulatory matters.
4. Identify new or updated policies, provide recommendations, and offer professional opinions on regulatory changes through blogs, webinars, etc.

Qualifications

1. College degree in Biological Science, Public Health, Regulatory Science, or related field; Masters or PhD preferred.
2. Reputation as an emerging leader with sustained performance and accomplishments.
3. Proficiency with MS Office applications.
4. Basic understanding of CRO operations, scientific/clinical data, terminology, and drug development process.

Additional Details

• Seniority Level: Mid-Senior level
• Employment Type: Full-time
• Industry: Pharmaceutical Manufacturing
• Location: Remote (Europe)