Senior specialist in Clinical Trial Supply Management

Location: Gdansk 80-309, Poland, Poland 
Contract type: Permanent 
Job ID: 2271 

Are planning and distribution some of your key drivers? Would you like an essential role making sure our Investigational Medicinal Products arrive at site in time and at the highest quality standard?  

You will become part of LEO Pharma Clinical Supply Management. We are a team of five professionals dedicated to facilitating high quality clinical trial supply. We work closely with departments such as Clinical Project Management and Quality, Product Formulation & Support, Regulatory Affairs and more ensure close collaboration and a smooth process. 

"By joining our team, you can look forward to a global dynamic set-up and becoming part of a highly supportive team were we share insights, have a good collaboration and foster a welcoming atmosphere,” – say your future colleagues. 

An essential role for advancement of clinical trials & development of life-changing therapies 

Your responsibility entails independently planning and coordinating clinical supply activities for all development phases, both in-house and outsourced trials including maintaining compliance with regulatory guidelines. 
Tasks associated: 

•    Reviewing overall clinical trial protocols and related documents.
•    Developing efficient packaging designs and visit schedules.
•    Building and maintaining accurate clinical supply demands aligned with protocol requirements and key study parameters.
•    Implementing optimal resupply strategies with proactive planning and appropriate lead-time.
•    setting up and maintaining Interactive Response Technology (IRT) Systems.
•    Consolidating and supervising clinical trial budgets in collaboration with key stakeholders.
•    Collaborating effectively across various organizational levels, functions, and geographies to achieve goals and objectives. 

You will also take on project responsibilities, ensuring collaboration between various departments and external vendors. 
This is an opportunity to make a significant impact on the success of clinical trials and contribute to the development of life-changing therapies and have a central role in overseeing the management of clinical trial supplies.

Who are you?

We are looking for you who can bring hands on experience with the associated task as, these elements will be central in this position. Furthermore, we imagine that you have: 

•    A degree in a relevant field (e.g., engineering, chemistry, pharmacy) 
•    5-8 years of experience in the pharmaceutical industry
•    Clinical supply management experience and knowledge of Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and Good Clinical Practice (GCP). 
•    Possesses professional proficiency in English, both written and spoken will be vital. 

Would you like to join our team? 

We will be processing applications on a continuous basis, so apply via the online portal as soon as possible. 

For additional information, please contact Andrea Beltran Olesen, Head og Clinical Project Management at OARDK@leo-pharma.com. 

We hope to hear from you!