Auf einen Blick
- Aufgaben: Lead regulatory affairs projects and manage submissions in a dynamic environment.
- Arbeitgeber: Join Boehringer Ingelheim, a family-owned company focused on innovative healthcare solutions.
- Mitarbeitervorteile: Enjoy flexible working hours, additional off-days, and comprehensive health promotion.
- Warum dieser Job: Be part of a diverse team driving breakthrough therapies with a strong focus on innovation.
- Gewünschte Qualifikationen: Experience in clinical development and regulatory affairs is essential; fluency in English required.
- Andere Informationen: This is a limited contract position for 12 months with opportunities for personal growth.
Das voraussichtliche Gehalt liegt zwischen 46305 - 64700 € pro Jahr.
Regulatory Affairs Operations Manager (m/f/d), limited contract 1120 Meidling Job ID 18376 Job Level Experienced professionals Functional area Medicine / regulatory affairs Schedule Full-time Our Company At Boehringer Ingelheim we develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company, we focus on long-term performance. We believe that, if we have talented and ambitious people who are passionate about innovation, there is no limit to what we can achieve; after all, we started with just 28 people. Now, we are powered by 50,000 employees globally who nurture a diverse, collaborative and inclusive culture. The position As of now we are seeking a Regulatory Affairs Operations Manager to join our team in RCV (Regional Center Vienna) for 12 months. This role requires a dynamic individual who is a fast learner, can handle complexity, and has a strong background in clinical development, clinical trial applications, and regulatory affairs. Tasks & responsibilities Lead and manage regulatory affairs (RA) projects, ensuring they are completed on time Serve as a business partner for Clinical Development & Operations Manage and supervise DSUR submissions within the RCV Stay updated on the latest digital trends and integrate them into our processes where applicable Support and conduct RA-specific trainings using state of the art methods and prepare and adjust corresponding training materials Maintain and manage RA-internal databases in scope, ensuring all data is accurate and up to date Requirements Proven experience in clinical development and clinical trial applications Experience in regulatory affairs, preferably within the pharmaceutical industry Ability to manage and lead projects effectively Strong affinity for database management and regulatory intelligence Fluent in English, German is an asset Your Benefits Flexible working time models/home office depending on the position Additional off-days (bridge-days) for more leisure time Staff restaurant with a variety of lunch options for your daily well-being Position specific training opportunities for your personal and professional growth Comprehensive health promotion, sustaining your health in the best possible way The minimum gross annual salary according to the collective bargaining agreement for this position is EUR 46.305 (full time). For the actual salary the industry benchmark as well as your qualifications and experiences are taken into consideration. We are looking forward to receiving your application online! By uploading your application documents via our application portal, we can treat your data confidentially and in compliance with the GDPR. Do you have any additional questions about the position? Your HR Recruiting Manager for this position is Katrin Spögler. On our career site you will find further information about us as an employer as well as information about the application process or our diverse divisions. Take a look behind the scenes and get an insight into our day-to-day business. Apply Now
Boehringer Ingelheim RCV GmbH & Co KG | Regulatory Affairs Operations Manager (m/f/d), limited contract Arbeitgeber: Boehringer Ingelheim RCV GmbH & Co KG
Kontaktperson:
Boehringer Ingelheim RCV GmbH & Co KG HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Boehringer Ingelheim RCV GmbH & Co KG | Regulatory Affairs Operations Manager (m/f/d), limited contract
✨Tip Number 1
Familiarize yourself with the latest trends in regulatory affairs and clinical development. This knowledge will not only help you during the interview but also demonstrate your commitment to staying updated in a fast-paced industry.
✨Tip Number 2
Network with professionals in the regulatory affairs field, especially those who have experience at Boehringer Ingelheim or similar companies. Engaging with them can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific projects you've managed in the past, particularly those related to clinical trial applications. Highlighting your project management skills will be crucial for this role.
✨Tip Number 4
Showcase your ability to work collaboratively by preparing examples of how you've partnered with other departments in previous roles. This will align well with the company's emphasis on teamwork and collaboration.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Boehringer Ingelheim RCV GmbH & Co KG | Regulatory Affairs Operations Manager (m/f/d), limited contract
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Regulatory Affairs Operations Manager position. Understand the key responsibilities and required qualifications to tailor your application accordingly.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in clinical development and regulatory affairs. Provide specific examples of projects you have managed or contributed to that align with the job requirements.
Showcase Your Skills: Demonstrate your ability to handle complexity and manage projects effectively. Mention any relevant skills such as database management and regulatory intelligence that are pertinent to the role.
Prepare a Strong Cover Letter: Craft a compelling cover letter that not only outlines your qualifications but also expresses your passion for innovation and your alignment with Boehringer Ingelheim's values. Make it personal and engaging.
Wie du dich auf ein Vorstellungsgespräch bei Boehringer Ingelheim RCV GmbH & Co KG vorbereitest
✨Show Your Regulatory Knowledge
Make sure to brush up on your knowledge of regulatory affairs, especially in the pharmaceutical industry. Be prepared to discuss specific regulations and how they impact clinical development and trial applications.
✨Demonstrate Project Management Skills
Since the role involves managing regulatory affairs projects, be ready to share examples from your past experiences where you successfully led projects. Highlight your ability to handle complexity and ensure timely completion.
✨Emphasize Your Training Experience
The position requires conducting RA-specific trainings. Prepare to talk about any training or mentoring experiences you've had, and how you can apply state-of-the-art methods to enhance learning.
✨Stay Updated on Digital Trends
Show your enthusiasm for integrating digital trends into regulatory processes. Discuss any relevant tools or technologies you are familiar with and how they can improve efficiency in regulatory affairs.