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- Aufgaben: Guide teams through clinical development and regulatory submissions for innovative projects.
- Arbeitgeber: Join a leading firm in the pharmaceutical industry, shaping the future of healthcare.
- Mitarbeitervorteile: Enjoy a hybrid work model with flexibility and a collaborative environment.
- Warum dieser Job: Be at the forefront of groundbreaking projects that impact patient lives globally.
- Gewünschte Qualifikationen: Advanced degree in life sciences and 10+ years in pharmaceutical development required.
- Andere Informationen: Experience with EU and US regulations is a plus; strong communication skills are essential.
Das voraussichtliche Gehalt liegt zwischen 72000 - 108000 € pro Jahr.
Clinical/Regulatory Consultant
Location: Munich, Germany – Hybrid
About the Role
In this matrix-structured role, you will provide strategic guidance and expertise to development teams working on a variety of cutting-edge projects, including small molecules, biologicals, and ATMPs. You will be involved in all stages of development, from pre-clinical research to regulatory submissions (MAA, NDA/BLA).
Key Responsibilities:
- Offer strategic regulatory advice and support to project teams.
- Oversee all clinical development aspects within project teams.
- Develop and execute a comprehensive global regulatory plan.
- Lead the development and implementation of the global agency interaction strategy.
Qualifications:
Advanced degree in life sciences, medicine, or veterinary medicine. Minimum of 10 years of experience in pharmaceutical development. Proven track record in strategic clinical development and regulatory affairs (experience in people management is not sufficient). Experience working across different pharmaceutical companies and/or regulatory authorities (a plus). Excellent communication and interpersonal skills, with the ability to explain complex development scenarios. Strategic thinking, solution-oriented approach, and strong problem-solving skills. Ability to work independently, manage multiple tasks under pressure, and prioritize effectively. Experience with EU and US regulatory procedures is preferred.
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Principal Consultant - Clinical Arbeitgeber: Barrington James Limited
Kontaktperson:
Barrington James Limited HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Principal Consultant - Clinical
✨Tip Number 1
Netzwerke sind entscheidend! Nutze Plattformen wie LinkedIn, um dich mit Fachleuten aus der Pharma- und Regulierungsbranche zu vernetzen. Suche gezielt nach Personen, die in ähnlichen Positionen arbeiten oder bei Unternehmen, die dich interessieren.
✨Tip Number 2
Informiere dich über aktuelle Trends und Entwicklungen im Bereich klinische Forschung und regulatorische Angelegenheiten. Zeige in Gesprächen, dass du auf dem neuesten Stand bist und verstehst, wie sich die Branche verändert.
✨Tip Number 3
Bereite dich darauf vor, deine Erfahrungen in der strategischen klinischen Entwicklung klar und prägnant zu kommunizieren. Überlege dir konkrete Beispiele, die deine Fähigkeiten und Erfolge in früheren Projekten verdeutlichen.
✨Tip Number 4
Sei bereit, Fragen zu deiner Herangehensweise an komplexe Probleme zu beantworten. Denke an Situationen, in denen du kreative Lösungen gefunden hast, und sei bereit, diese zu teilen, um deine Problemlösungsfähigkeiten zu demonstrieren.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Principal Consultant - Clinical
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description and understand the key responsibilities and qualifications required for the Principal Consultant - Clinical position. Tailor your application to highlight relevant experiences.
Highlight Relevant Experience: In your CV and cover letter, emphasize your 10+ years of experience in pharmaceutical development, particularly in strategic clinical development and regulatory affairs. Provide specific examples of projects you've worked on that align with the role.
Showcase Communication Skills: Since excellent communication and interpersonal skills are crucial for this role, include examples in your application that demonstrate your ability to explain complex scenarios clearly and effectively.
Tailor Your Application: Customize your cover letter to reflect your understanding of the company's needs and how your background makes you a perfect fit for the role. Mention your experience with EU and US regulatory procedures if applicable.
Wie du dich auf ein Vorstellungsgespräch bei Barrington James Limited vorbereitest
✨Showcase Your Strategic Thinking
In this role, strategic thinking is crucial. Be prepared to discuss specific examples from your past experiences where you successfully developed and executed regulatory plans or navigated complex clinical development scenarios.
✨Demonstrate Your Regulatory Knowledge
Make sure to highlight your understanding of EU and US regulatory procedures. Discuss any relevant experiences you have had with regulatory submissions like MAA or NDA/BLA, as this will show your expertise in the field.
✨Communicate Clearly and Effectively
Given the importance of communication in this role, practice explaining complex concepts in a simple manner. Prepare to articulate how you would convey strategic advice to project teams and stakeholders.
✨Prepare for Behavioral Questions
Expect questions that assess your problem-solving skills and ability to manage multiple tasks under pressure. Use the STAR method (Situation, Task, Action, Result) to structure your responses and provide clear, concise examples.
