Finde einen Job 
Finde eine Ausbildung 
Top Arbeitgeber 
Top Universitäten 
Für Unternehmen Auf einen Blick
- Aufgaben: Provide strategic guidance on innovative drug development projects.
- Arbeitgeber: Join a dynamic organization leading in innovative drug development.
- Mitarbeitervorteile: Enjoy a competitive salary, relocation support, and professional development opportunities.
- Warum dieser Job: Work on cutting-edge projects in a non-client facing role with a focus on expertise.
- Gewünschte Qualifikationen: Advanced degree in life sciences and 10+ years in pharmaceutical development required.
- Andere Informationen: Experience with EU and US regulatory procedures is preferred.
Das voraussichtliche Gehalt liegt zwischen 72000 - 84000 € pro Jahr.
Job Description
Clinical/Regulatory Consultant
Location: Munich, Germany – Hybrid
The Company is a dynamic organization at the forefront of innovative drug development. We offer a unique opportunity for a highly motivated and experienced Clinical/Regulatory Consultant to join our cross-functional development teams.
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.
Benefits & Perks:
- Competitive salary, with no pre-set cap (negotiated based on experience).
- Comprehensive relocation package, including assistance with finding accommodation, schooling, and navigating bureaucratic processes.
- Opportunity for continuous professional development through exposure to diverse, cutting-edge projects, not through hierarchical advancement.
- Non-client facing role, allowing you to focus on your expertise.
#LI-OG1#J-18808-Ljbffr
Principal Consultant - Clinical Arbeitgeber: Barrington James
Kontaktperson:
Barrington James HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Principal Consultant - Clinical
✨Tip Number 1
Familiarize yourself with the latest trends and regulations in clinical development and regulatory affairs. This will not only help you understand the role better but also demonstrate your commitment to staying updated in this fast-paced field.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who have experience in regulatory submissions. Engaging in discussions or attending relevant conferences can provide valuable insights and connections that may benefit your application.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences where you successfully navigated complex regulatory challenges. Highlighting these instances during interviews can showcase your problem-solving skills and strategic thinking.
✨Tip Number 4
Research our company’s recent projects and initiatives in drug development. Being knowledgeable about our work will allow you to tailor your conversations and show how your expertise aligns with our goals.
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 innovative approach to drug development. Mention how your strategic thinking and problem-solving skills can contribute to their projects.
Wie du dich auf ein Vorstellungsgespräch bei Barrington James vorbereitest
✨Understand the Regulatory Landscape
Make sure you are well-versed in both EU and US regulatory procedures. Familiarize yourself with recent changes and trends in drug development regulations, as this knowledge will be crucial during your interview.
✨Showcase Your Strategic Thinking
Prepare to discuss specific examples where you've developed and executed a comprehensive global regulatory plan. Highlight your strategic approach to problem-solving and how it has positively impacted project outcomes.
✨Communicate Complex Ideas Clearly
Practice explaining complex clinical development scenarios in simple terms. The ability to communicate effectively with cross-functional teams is essential, so demonstrate your interpersonal skills during the interview.
✨Highlight Your Experience Across Companies
If you have experience working with different pharmaceutical companies or regulatory authorities, be sure to mention it. This background can set you apart and show your adaptability in various environments.
