Associate Project Manager Clinical Supply Chain
Location: NetherlandsSIRE 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 Noord-Brabant Netherlands.
This company discovers, develops and produces new innovative human therapeutics that improve the life expectancy of humanity.
ROLE DESCRIPTION
As associate project manager you will support the project managers clinical supply chain. Their main objective is to timely, efficient and effective lead the global design and set up of clinical supply chains for the assigned clinical programs/studies.
RESPONSIBILITIES
- Initiating and maintaining change control management system to introduce new investigational products at the site. Gathering input from appropriate stakeholders, hosting stakeholders meeting, compiling the company site readiness project plan and following up on assigned pre- and implementation tasks to adhere to overall project timelines.
- Initiating and routing clinical artwork creation request forms; tracking project status with clinical labeling associate and following up on outstanding queries. Facilitate discussion to resolve issues and elevate if project timelines are jeopardized.
- Functions as central point of contact for ERP (SAP) readiness. Initiate label, finished drug product material number request plus bill of material (BOM) and ensure timely availability to adhere to overall project timelines by tracks process flow in SAP.
- Creating, maintaining and updating third party depot and cross dock plans. Routing documents via quality systems to ensure timely availability of depots and cross docks readiness to support global study footprint. -
- Updating and maintaining product specification file throughout the life cycle of the clinical trial.
- Routing other documents through the companys Quality Systems as per the overall project plan
REQUIREMENTS
- 1-4 years of experience in Supply Chain
- Knowledge of Clinical Supply Chain
- Good communication skills in English
- Experience with MS Office and preferably SAP
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Demi Ridder.
