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- Aufgaben: Lead the growth of Veeva’s Regulatory Information Management market and drive innovative solutions.
- Arbeitgeber: Join Veeva, a global leader in life sciences technology, committed to diversity and inclusion.
- Mitarbeitervorteile: Enjoy a collaborative culture, opportunities for travel, and the chance to present at industry events.
- Warum dieser Job: Be part of a dynamic team shaping the future of regulatory applications in life sciences.
- Gewünschte Qualifikationen: 5+ years in regulatory processes; experience in consulting and software sales is a plus.
- Andere Informationen: Veeva values diverse perspectives and offers support for applicants with disabilities.
Das voraussichtliche Gehalt liegt zwischen 72000 - 84000 € pro Jahr.
This Director role requires a deep understanding of the global life sciences Regulatory Operations space, RegOps business processes and supporting technology solutions. This role will be responsible for growing Veeva’s Regulatory Information Management market share. In this role, the individual will have the opportunity to work with a team of Life Sciences industry and technology A-players, who, together, are bringing the next generation of Regulatory applications and capabilities to the life sciences industry.
What You’ll Do
- Responsible for growing and sustaining the Regulatory market for the Vault RIM applications including Vault Registrations, Submissions, Submissions Archive, and Submissions Publishing
- Provide thought leadership, strategy, and direction to account teams in driving new opportunities in the Regulatory space
- Provide business and technology guidance to the product team in support of new or enhanced features and functionality in regulatory applications
- Develop strategy and messaging for customer adoption of new features and functionality for new and existing customer base
- Coordinate resources across the customer lifecycle from sales to delivery and beyond
- Present at industry conferences, lead webinars, and author articles for industry publications
Requirements
- 5+ years of experience with regulatory processes and technology for submission document authoring, submission publishing / validation / viewing, registration and commitment tracking, and regulatory document archiving
- 3+ years of experience consulting for the regulatory operations area of a life sciences company
- 3+ years of experience selling software and / or services to life sciences organizations
- Proven ability to innovate across business processes and technology solutions
- Ability to hold strategic conversations with heads of regulatory and IT regarding the regulatory applications and their use within Regulatory execution
- Understanding of global drug development & regulatory process
- Ability to travel for customer meetings and presentations
Nice to Have
- 2+ years of experience working for a Regulatory or content management software company in a Product, Consulting or Services function
- 3+ years of experience directly working with Registration Management, Submissions, Submissions Archive, and Publishing technologies
- Experience with regulatory data standards, such as xEVMPD and IDMP, a plus
- Proven track record of thought leadership through industry presentations, publications, or other mechanisms
Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world. As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams. If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at.
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Financial Regulatory | Volljurist (m / w / d) Arbeitgeber: Flex Suisse GmbH
Kontaktperson:
Flex Suisse GmbH HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Financial Regulatory | Volljurist (m / w / d)
✨Tip Number 1
Familiarize yourself with the latest trends and technologies in regulatory operations within the life sciences sector. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Network with professionals in the regulatory space, especially those who have experience with Veeva’s products. Engaging in conversations with industry experts can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples of how you've driven innovation in regulatory processes or technology solutions in your previous roles. Highlighting your achievements will set you apart from other candidates.
✨Tip Number 4
Consider attending industry conferences or webinars related to regulatory operations. Not only will this enhance your knowledge, but it also provides opportunities to connect with potential employers and showcase your expertise.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Financial Regulatory | Volljurist (m / w / d)
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description and understand the key responsibilities and requirements. Tailor your application to highlight your relevant experience in regulatory processes and technology.
Highlight Relevant Experience: In your CV and cover letter, emphasize your 5+ years of experience with regulatory processes, especially in submission document authoring and validation. Provide specific examples of how you've contributed to similar roles in the past.
Showcase Thought Leadership: If you have experience presenting at industry conferences or authoring articles, make sure to include this in your application. This aligns with the company's emphasis on thought leadership in the regulatory space.
Customize Your Cover Letter: Write a personalized cover letter that addresses Veeva's mission and values. Discuss how your background in life sciences and regulatory operations can contribute to their goals, particularly in growing the Regulatory Information Management market.
Wie du dich auf ein Vorstellungsgespräch bei Flex Suisse GmbH vorbereitest
✨Understand Regulatory Processes
Make sure you have a solid grasp of regulatory processes and technology related to submission document authoring and publishing. Be prepared to discuss your experience in these areas and how it relates to the role.
✨Showcase Your Thought Leadership
Highlight any instances where you've provided thought leadership in the regulatory space. This could include presentations, articles, or innovative strategies you've implemented in previous roles.
✨Prepare for Strategic Conversations
Since this role involves holding strategic conversations with heads of regulatory and IT, practice articulating your insights and recommendations clearly. Think about how you can add value to their operations.
✨Demonstrate Your Industry Knowledge
Familiarize yourself with current trends and challenges in the life sciences industry, especially regarding regulatory applications. Being able to discuss these topics will show your passion and commitment to the field.
