Keyrus – Clinical Trial Supply Manager – Belgique
Keyrus Life Science is looking for a Clinical Trial Supply Manager to join their team based in Waterloo !
The Clinical Trial Supply Manager is accountable for the set-up and follow-up of the logistical activities from the issue of a draft concept protocol till the overall vaccine reconciliation at study end.
This includes :
- the translation of study protocols into on operational demand ;
- the feasibility assessment for completion of logistical activities ;
- the definition of logistical operational strategies (supply, distribution, randomization,…) ;
- the set-up and follow-up of clinical supply related activities for a project or a group of studies ;
- the guaranty of alignement among the network of stakeholders, GMP operations and clinical operations (central and local) to support the delivery of clinical vaccines and ancillaries in timeat right quality and within agreed budget.
The scope of the work includes project management, leadership and oversight of both global and incountry activities, as well as authorship at some study documents.
We are looking for a profile who has a university degree in Biology, Biochemistry, Chemical Engineering, Bioengineering, Pharmacy, or other relevant discipline with a first experience in clinical research and/or clinical supply management. You are fluent in written and spoken English and have a good level of written and spoken French. You have excellent coordination skills and have a strong and overall clinical Project/Study knowledge. You are familial with GCP & GDP quality standards and are totally knowlodgeable about Clinical Trial Supplies Operations (Labelling/Pack/WH/Distribution).
What we offer
At Keyrus, thanks to the expertise of our people and external partners, each employee is welcomed with a varied integration program. You will join a dynamic and international environment with enthusiastic and professional colleagues.
We invest considerable time and resources in training our staff (technical and non-technical courses) to continuously support you in your personal and professional growth. On top of this, you will receive a complete salary package including attractive extra-legal benefits (company car, petrol card, meal vouchers, group insurance, hospitalization…) based on your background and experience.
Who we are
Keyrus Life Science is an international Consulting, Contract Research Organisation and Functional Services provider with a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our ‘human’ approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.
At Keyrus Life Science we’re proud of our commitment to delivering services of the highest quality, not only skillfully, efficiently and reliably, but also with sincerity and genuine care for our clients’ projects, priorities and reputation. Thus we maintain and advance our vision and our standards, all the while ensuring that we serve your interests better.
From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services.