Contrôleur Financier Global Markets (H / F)

Kyndryl; Paris; Sur place; EUR 60 000 - 80 000; Plein temps

Résumé du poste

Une entreprise innovante recherche un stratège réglementaire principal pour rejoindre une équipe dynamique et collaborative. Dans ce rôle, vous fournirez des services de conseil sur des questions réglementaires complexes, tout en maintenant la conformité et en soutenant le développement de feuilles de route réglementaires. Avec plus de 15 ans d'expérience dans le domaine, vous serez un leader émergent, apportant votre expertise à des projets critiques. Ce poste à temps plein, en télétravail, vous offre l'opportunité de contribuer à des défis passionnants dans le domaine de la recherche clinique et de faire avancer votre carrière dans un environnement reconnu pour son excellence.

Qualifications

• 15+ ans d'expérience en affaires réglementaires ou stratégie.
• Maîtrise des principes scientifiques et des concepts.

Responsabilités

• Fournir des services de conseil pour des problèmes réglementaires complexes.
• Participer à l'élaboration de stratégies opérationnelles.

Connaissances

Compétences en communication

Résolution de problèmes

Connaissances scientifiques

Compétences organisationnelles

Formation

Diplôme en sciences biologiques

Master ou Doctorat

Outils

MS Office

Description du poste

Description de poste

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 best 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 not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research. Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.

This would be a full-time consultancy role, working remotely.

Principal Regulatory Strategist Responsibilities

1. Provide consulting and advisory services for complex regulatory issues or projects.
2. Author and maintain documentation as required to sustain regulatory compliance.
3. Provide senior technical review for complex regulatory projects.
4. Conduct regulatory intelligence gathering to support development of regulatory roadmaps, complex feasibility assessments, and other regulatory intelligence reports.
5. Participate on project teams and provide expertise on related regulatory matters.
6. Clearly and accurately convey information to peers, supervisors, and other stakeholders.
7. Participate in the implementation of new/updated operational strategies to comply with new/updated policies and recommendations.
8. Identify new/updated policies and recommendations and may provide professional opinions on the impact of regulatory changes to MMS and Clients (from the desk of, blogs, webinars, etc.).

Requirements

1. College graduate in Biological Science, Public Health, Regulatory Science, or related field, or related experience; Masters or PhD preferred.
2. Minimum of 15 years’ experience in Regulatory Affairs or Strategy or similar field required, including experience with Marketing Applications (EMA).
3. Expert knowledge of scientific principles and concepts.
4. Reputation as an emerging leader in the field with sustained performance and accomplishment.
5. Proficiency with MS Office applications.
6. Hands-on experience with clinical trial and pharmaceutical development preferred.
7. Good communication skills and willingness to work with others to clearly understand needs and solve problems.
8. Excellent problem-solving skills.
9. Good organizational and communication skills.
10. Basic understanding of CROs and scientific and clinical data/terminology, and the drug development process.