Head of Clinical Trial Supplies
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Ballerup
Can you spearhead LEO Pharma’s business critical management of clinical trials supplies?
LEO Pharma has set the ambitious goal to become the world’s preferred dermatology care partner and to improve the quality of life for millions of patients around the world. Our approach is a growth and innovation strategy, with the aspiration of growing double-digit revenue above industry average and develop best-in-class and first-in-class compounds. To succeed, we invest massively in R&D and as a result, our clinical activities are growing rapidly. You will join LEO Pharma at a very exciting period in the company’s history, and you can look forward to significant influence and impact on shaping of your own job as well as the overall direction for Clinical Trial Supply and Global Clinical Operations.
Management of IMP outsourced related activities across phase I-IV
As Head of Clinical Trial Supply your focus will be threefold. Firstly, you will ensure supplies to LEO Pharma’s global clinical studies. Secondly, you will establish and nourish solid relations to stakeholders internally and externally, to facilitate high performance success rate of your team. Your collaboration must be based on transparency, trust, and the will to achieve common goals.
Finally, you must guide, coach, and motivate your team to help them accomplish their best game.
Your responsibility includes to:
- Head a team of 7 clinical supply professionals
- Build and nurture a team culture of mutual trust, respect, fun, cooperation, and common drive for results.
- Coach, guide and develop your team members in a positive and inspiring way.
- Develop and implement the Global Clinical Operation’s strategy towards 2030.
- Set the direction to build successful relationships internally and with external strategic partners.
- Ensure effective collaboration across different organizational levels, functions, and geographies to realize goals and objectives.
- Build a solid communication strategy to ensure transparent communication and alignment of expectations between internal and external stakeholders.
- Identify organizational needs to ensure correct trial supply support.
- Set the direction and establishment of tools to facilitate and drive processes within clinical trial supply.
- Strive to constantly optimize the area with the aim of being best in class Clinical Trial Supplies team.
You will collaborate and liaise closely with multiple internal stakeholders such as Senior Management, Clinical Project Managers, Clinical Operations Leads, Quality, CMC, Global Product Supply, etc. Your road to success will to a large extent depend on your ability to deliver advice in a respectful and always professional way – you must be able to balance when to stand your ground and when to compromise and seek the pragmatic solution. Motivate your team to follow this path is essential for this position.
Experienced manager in Pharma R&D and with solid leadership skills
You have a life science, Business Administration, or equivalent degree at Master’s level. Further, you have a minimum of 5 years’ clinical development experience including clinical trial supplies, good understanding of IRT systems and an overall GMP understanding.
You have experience as people manager and you are known for your open-minded and positive leadership style. You drive for results and even though you thrive on setting the direction and taking the lead, nothing motivates you like accomplishing results by strong team work. Additionally, you have the toolbox to build, motivate and inspire high performance teams with a common drive for success. In this you benefit from your excellent communication skills that enable you to bring your messages across in an easy understandable way, written as spoken.
As part of a fast-paced organisation you must also thrive in an environment of change and be able to navigate in a constructive way without having manuals and procedures for each and every process.
You can look forward to travel 5-10 days per year (in normal non-Corona times). Most of the travelling you plan yourself to match your calendar.
Clinical Trial Supplies – your new team
Your will join a team of experienced and very dedicated clinical trial specialists. We are 6 in Ballerup where you will be based, and we have one colleague in the US. We are part of Global Clinical Operations that is responsible for conducting all LEO Pharma sponsored clinical trials from phase I-IV. Our working environment is friendly and welcoming and characterised by a helpfulness and team spirit. We believe that trust and respect are the foundation for the greatest results.
Contact and application
Please apply at our website. The deadline is 20 April 2022. If you have any questions, you are very welcome to contact Head of External Clinical Project Management Andrea Beltrán Olesen on +45 3120 5143.
We look forward to receiving your application.
About LEO Pharma
LEO Pharma helps people achieve healthy skin. By offering care solutions to patients in more than 100 countries globally, LEO Pharma supports people in managing their skin conditions. Founded in 1908 and owned by the LEO Foundation, the healthcare company has devoted decades of research and development to delivering products and solutions to people with skin conditions. LEO Pharma is headquartered in Denmark and employs around 6,000 people worldwide. For more information, visit www.leo-pharma.com.
Information og data
Denne ledige stilling har jobtypen "Afdelingsleder", og befinder sig i kategorien "Ledelse og personale".
Arbejdsstedet er beliggende i Ballerup.
Jobbet er oprettet på vores service den 23.3.2022, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Afdelingsleder
- Ballerup
- Onsdag den 20. april 2022
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