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. You will be part of the clinical research department.
ROLE DESCRIPTION
As associate project manager you will support the project managers clinical supply chain. The main objective of the role is the timely, efficient, effective and set up of clinical supply chains for the assigned clinical programs/studies. Different projects per country/cluster have to be managed in order to ensure global supplies at the start of the different studies. Your task will be to assist in the completion of different subtasks and ensuring overall timelines and deadlines are met.
RESPONSIBILITIES
- Gathering input from different stakeholders and hosting stakeholders meetings.
- Following up on assigned implementation tasks to adhere to overall project timelines.
- Tracking project status and following up on outstanding queries.
- Facilitate discussion to resolve issues and elevate if project timelines are not met.
- Point of contact for ERP (SAP) readiness and ensure timely availability of materials to adhere to overall project timelines by tracks process flow in SAP.
- Routing documents via quality systems to ensure timely availability of depots and cross docks readiness to support global study footprint.
- Updating and maintaining a product specification file throughout the life cycle of the clinical trial.
REQUIREMENTS
- Bachelor degree or equivalent in supply chain or logistics
- Minimum 2 years relevant working experience within a regulated industry (pharmaceuticals, biotechnology)
- Experience in project management and working in a regulated industry
- Advanced experience with MS Office and SAP
- Fluent in English (Written and Verbal)
- Excellent communication, facilitating and issue resolution skills
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.
