Clinical Supply Chain Manager
Location: BelgiumSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Pharmaceutical organization, based in Antwerpen Belgium.
Top tier pharmaceutical American multinational. The organization provides the world with products and services to improve the health and well-being of people.
ROLE DESCRIPTION
Temporary role of initial 1 year, seconded via SIRE Life Sciences.
For this position you are responsible for the management of clinical supplies during the execution phase of clinical trials consistent with GMP guidelines. Responsible for the management of all clinical supplies during trial execution (large and small molecules and for all phases of clinical trials).
RESPONSIBILITIES
- Adopt supply strategies in view of changes in trial execution and ensure a seamless transition from study design phase.
- Assess clinical study recruitment rates and ensure supply planning is adopted accordingly.
- Utilize business tools to manage inventories at depots and sites and ensure on-time delivery with minimal overage of clinical supplies.
- Conduct issue resolution activities for supply aspects of clinical studies (e.g., packaging, distribution).
- Establish and modify trial specific distribution agreements
- Member of appropriate clinical trial team.
- Develop strong internal collaboration with stakeholders to ensure customer satisfaction.
- Interface with Global Trial Managers.
- Manage trial supply budget.
- Develop excellent working relationships with the other groups within Supply Management.
REQUIREMENTS
- Bachelor or Master’s degree
- 4-6 years experience preferably in a clinical supply related role
- Experience with clinical supply demand management tools (e.g., tcVisualize, IVRS, SAP)
- General knowledge of GxP principles
- Intermediate to advanced software skills (e.g., Microsoft Excel, Powerpoint)
- Excellent written and verbal communication skills
- Strong planning and cross-functional coordination skills
- Strong attention to detail
- Ability to work independently with some coaching
- Ability to multi-task and manage complexity
- Ability to work in a high pressure environment
- Solution oriented
- Exceptional collaboration skills
- Integrity and Credo Based-actions
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Pascha Groot.
