Clinical Trial Supply Manager

Contenido de trabajo

Take the chance to join a fast-growing and super dynamic team. The Clinical Supply team at Keyrus Life Science is bursting with new exciting projects and is always looking to expand since its beginning. If you want to be part of a big family, grow professionally and make patients matter, this is the place to be!

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.

Job Description

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, Good Manufacturing Practices (GMP) operations and clinical operations (central and local) to support the delivery of clinical vaccines and ancillaries in time at 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.

Profile

• You hold a Master’s degree in Biology, Biochemistry, Chemical Engineering, Bioengineering, Pharmacy, or other relevant discipline.
• You have at least 3 years of experience in a Clinical Supply Manager roleor any other related responsibilities (e.g. Lab Study Manager).
• You have excellent coordination skills and have a strong and overall clinical Project/Study knowledge.
• You are familial with Good Clinical Practices (GCP) & Good Distribution Practices (GDP) quality standards and are totally knowlodgeable about Clinical Trial Supplies Operations (Labelling/Pack/Warehouse/Distribution).
• Fluentin written and spoken English.
• Immediately available

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.

Excited for more information?

Contact: Andrea Baetens - 0494 05 37 29