Head Regulatory Information Management (m/f/d)
UK Visa Sponsorship Analytics
Analytics are greyed out due to low classification confidence (35.0%).
Occupation Type
Information technology directors
Occupation Code Skill LevelHigher Skilled
Sponsorship Salary Threshold
£86,000
(£44.10 per hour)
Occupation rate applies
Above analytics are generated algorithmically based on job titles and may not always be the same as the company's job classification. You can also check detailed occupation eligibility, and salary criteria on our UK Visa Eligible Occupations & Salary Thresholds page.
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Description
Professional | Permanent | Full-time | Hybrid
If you’re passionate about changing lives for the better, this is the opportunity you’ve been waiting for. In Research & Development, we’re continuously exploring innovative new treatment options to make a stronger, more positive impact on the lives of the patients we serve. You’ll work with talented colleagues in a state-of-the-art Research & Development environment, developing innovative medicines that change the life of patients for the better and help us make progress towards our vision of a world free of pain. Join us today, and discover the difference you can make.
What The Job Looks Like
Each day you'll enjoy a variety of challenges, such as:
If you’re passionate about changing lives for the better, this is the opportunity you’ve been waiting for. In Research & Development, we’re continuously exploring innovative new treatment options to make a stronger, more positive impact on the lives of the patients we serve. You’ll work with talented colleagues in a state-of-the-art Research & Development environment, developing innovative medicines that change the life of patients for the better and help us make progress towards our vision of a world free of pain. Join us today, and discover the difference you can make.
What The Job Looks Like
Each day you'll enjoy a variety of challenges, such as:
- Delivering high-quality regulatory information management services for Grünenthal, including:
- RIM Product Championship (functional expertise, change management, training, and adoption of functionalities)
- RIM Process Management (harmonized, effective, and continuously improved business processes)
- RIM Data Management (effective, compliant, and aligned data management processes & standards)
To make the most of this role and truly thrive, you should have:
- University degree in science, technology, or equivalent experience
- 10+ years of experience in regulatory information management within the pharmaceutical industry
- Strong knowledge of RIM processes across development and marketed products (EU & US required; LATAM a plus)
- In-depth understanding of relevant regulatory standards and regulations (e.g. IDMP, xEVMPD, eCTD, ESMP)
- 5+ years of hands-on experience with Veeva Vault RIMS and its business processes
- Experience with multiple RIM technologies and digital trends in Global Regulatory Affairs
- Global regulatory experience with a focus on EU and US
- Proven leadership and people development experience, driving high-performing teams
- Solid experience in budget, vendor, and contract management
- Strong project, people, change, and stakeholder management skills
- Excellent communication, negotiation, and presentation skills
"At this moment, we are in an exciting time of change, modernizing our RIM landscape. Join us to become part of the adventure!"
Silke Thömmes , the Hiring Manager