Operador / A Temporal Centro De Control - Dispatching

buscojobs España; Valencia; A distancia; EUR 10.000 - 30.000; Jornada completa

Descripción de la vacante

A leading clinical research organization is seeking a Principal Regulatory Strategist to provide consulting services on complex regulatory issues. This full-time remote role requires a college degree and a minimum of 15 years of experience in Regulatory Affairs. Join a supportive team recognized for its exceptional culture and employee retention.

Formación

• Minimum 15 years’ experience in Regulatory Affairs or Strategy.
• Expert knowledge of scientific principles.
• Proficiency in MS Office and experience with clinical trials preferred.

Responsabilidades

• Provide consulting and advisory services for complex regulatory issues.
• Author and maintain documentation for regulatory compliance.
• Conduct senior technical reviews for regulatory projects.

Conocimientos

Communication

Problem-solving

Organizational skills

Collaborative mindset

Educación

College degree in Biological Science, Public Health, Regulatory Science

Master’s or PhD preferred

Herramientas

MS Office

Descripción del empleo

EUR 10.000 - 30.000

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO).

We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry-leading employee retention rate.

We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges.

With a global footprint across four continents, MMS maintains an industry-leading customer satisfaction rating and fosters a collaborative and inclusive work environment where employees can thrive.

Join us at MMS and be part of a team shaping the future of clinical research.

This is a full-time, remote consultancy role.

Principal Regulatory Strategist Responsibilities

1. Provide consulting and advisory services for complex regulatory issues or projects.
2. Author and maintain documentation to ensure regulatory compliance.
3. Conduct senior technical reviews for complex regulatory projects.
4. Gather regulatory intelligence to support development of regulatory roadmaps, feasibility assessments, and reports.
5. Participate in project teams, providing expertise on regulatory matters.
6. Communicate clearly and accurately with peers, supervisors, and stakeholders.
7. Implement operational strategies to comply with new policies and recommendations.
8. Identify and analyze the impact of regulatory changes, providing professional opinions through blogs, webinars, etc.

Requirements

1. College degree in Biological Science, Public Health, Regulatory Science, or related field; Master’s or PhD preferred.
2. Minimum 15 years’ experience in Regulatory Affairs or Strategy, including experience with Marketing Applications (EMA).
3. Expert knowledge of scientific principles; recognized as an emerging leader in the field.
4. Proficiency in MS Office; experience with clinical trials and pharmaceutical development preferred.
5. Strong communication skills and collaborative mindset.
6. Excellent problem-solving and organizational skills.
7. Basic understanding of CRO operations, clinical data, and drug development processes.