Principal – Management Consultant, Regulatory

Job not on LinkedIn

🔥 5 hours ago

🗣️🇩🇪 German Required

Apply Now
Find Similar Remote Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Logo of MAIN5

MAIN5

51 - 200 employees

At MAIN5, we redefine consulting with a dynamic and forward-thinking approach, positioning ourselves as leaders in the ever-evolving landscape of the Life Sciences Industry. With over 60 dedicated professionals, we are committed to driving innovation and digital transformation for our clients. Our Core Values: Innovation, Expertise, and Excellence Innovation: In a world shaped by rapid advancements, MAIN5 stands at the forefront of industry trends. We embrace innovation as a guiding principle, ensuring our clients stay ahead in the competitive life science sector. Our commitment to cutting-edge technologies is unwavering, making us your strategic partner in navigating the digital age. Expertise: With a team of seasoned professionals, MAIN5 brings unparalleled expertise to the table. Our consultants are adept in Regulatory Affairs, Quality, Safety, Clinical, and other critical areas along the R&D value chain. We provide tailored solutions that align with your unique challenges, leveraging our deep industry knowledge to drive success. Excellence: At MAIN5, excellence is not just a goal; it's our standard. We pride ourselves on delivering tangible and sustainable results for our clients. Our track record showcasing a history of successful projects in Change Management, Business Process Management, System implementations, eLearning, Quality & Compliance that have empowered organizations to thrive in the face of complexity.

📋 Description

• Take responsibility for one or more projects • Lead a project team and ensure that expectations are met • Introduce and implement best practices and methodologies to create value for the client • Conduct workshops, gather requirements, manage vendor selection and execute data migrations • Act as the liaison between the company and software vendors • Improve business processes • Promote a culture of knowledge sharing • Identify and propose opportunities to improve team performance

🎯 Requirements

• More than 5–8 years of experience in the pharmaceutical industry • Expertise in Regulatory Operations and Regulatory Information Management • Deep understanding of regulatory processes and data • Expert in data management, including Data Governance and Master Data Management • Practical experience with xEVMPD and IDMP • Knowledge of relevant guidance, such as the EU IDMP Implementation Guide • Experience implementing and operating RIM systems • Development and execution of data migration strategies • Strong affinity for both business and technology

🏖️ Benefits

• Attractive compensation with bonus opportunities • Flexible working hours & remote work options • State-of-the-art equipment for office and remote work • Creative working environment & inspiring events • Regular international team meetings & company events • Secure position with long-term prospects

Apply Now

Similar Jobs

🕒 March 31

Veeva Systems

1001 - 5000

☁️ SaaS

⚕️ Healthcare Insurance

💊 Pharmaceuticals

Lead R&D consulting initiatives at Veeva, a life sciences innovator, building customer networks and managing project deliveries across Europe.