Clinical Supply Chain Specialist - Gosselies, België - iTeos Therapeutics

iTeos Therapeutics
iTeos Therapeutics
Geverifieerd bedrijf
Gosselies, België

1 maand geleden

Sophie Dubois

Geplaatst door:

Sophie Dubois

beBee Recruiter
Beschrijving

ABOUT ITEOS THERAPEUTICS, INC
iTeos Therapeutics is a publicly-traded (


NASDAQ:
ITOS), clinical-stage biopharmaceutical company dedicated to extending and improving the lives of patients with cancer by designing and developing next generation immunotherapies.


Based in Gosselies, Belgium and Watertown, MA, iTeos Therapeutics was founded out of the Ludwig Institute for Cancer Research (LICR) and the de Duve Institute (UClouvain) in 2011.


In March 2020, the Company completed a $125 million Series B2 financing, and in July 2020, we completed our IPO, raising over $230 million of gross proceeds.

In June 2021, the Company entered into a transformative $2.145 billion co-development and co-commercialization agreement with GSK for EOS-448, the Company's anti-TIGIT monoclonal antibody.

As a well-capitalized biotech company, we are positioned to continue to develop our clinical pipeline and maintain our investments in our discovery research team to leverage our innovative science to improve the lives of patients with cancer.


iTeos Therapeutics is now a world-class actor in the sector. To carry on its growth and reinforce its team, iTeos Therapeutics is looking for a Clinical Supply Chain Specialist.**
ROLE:Clinical Supply Chain Specialist**iTeos Therapeutics is actively looking for a Clinical Supply Chain Specialist (CSCS), you will work with project teams, vendors, and CMC to support the end-to-end clinical supply chain activity. Your knowledge of the clinical supply chain, GxP regulatory framework and deep understanding of the dynamics and interdependence of both medicinal product and clinical development will be critical for the development of supply strategies to advance iTeos' clinical pipeline.


The CSCS will support the Clinical Supply Chain Manager for the Global Clinical Supply deliverables and outcomes, as a point of contact to stakeholders across Clinical, Clinical Operations, CMC, Discovery, Quality Assurance and Regulatory Affairs to advance the development of the ON portfolio.

As the supply chain point of contact, you will provide broad consult on all aspects of clinical supply. The goal of these interactions is to meet the ever evolving and demanding needs of clinical trials. Through an understanding of clinical study design and drug supply risks.


MAIN RESPONSIBILITIES

  • Coordinate various supply chain vendors and services, in order to follow our continuous improvement goals.
  • Follow the operational activities of packaging, labeling, and distribution of clinical trial material for global clinical trials with the IMP vendors.
  • Maintain and track clinical supply inventory and expiration dates.
  • Coordinate notification to QA of clinical supply temperature excursion.
  • Assist IRT (Interactive Response Technology) development, user acceptance testing (UAT), as well as utilize the system to actively manage clinical trial material.
  • Coordinate the review, approval, and generation of clinical label text for study drug material.
  • Assist for all information regarding the global use of investigational material in clinical studies: Forecasting, Packaging, Distribution, Inventory Management, Project Management and Budgeting.
  • Close followup of invoices to ensure budget approved alignment.
  • Maximize tools knowledge to increase productivity, manage complexity, and improve forecast quality.

PROFESSIONAL EXPERIENCE/QUALIFICATIONS

  • Bachelor's degree, minimum of 35 years' experience in Pharmaceutical or Biotechnology Industry and in a clinical supply related role preferred.
  • Understanding of endtoend clinical supply chain activities.
  • Understanding of GxP concepts and impact to clinical supply.
  • Ability to develop forecasts and supply plans for investigational products incorporating expiry management and accounting for complex regulatory requirements.
  • Experience leveraging tools and systems to help with demand forecasting.
  • Experience with IRT systems and providing stakeholder input for IRT development.
  • Proficient knowledge of MS Office (Excel, PowerPoint, Project, etc).

OFFER

  • A stimulating position within a highpotential innovative biotech company.
  • The opportunity to work in a sciencedriven, dynamic, respectful, and professional environment.
  • A challenging scientific and business growth in which you get to bring your knowledge and skills.
  • A permanent contract with an attractive salary package in line with the position responsibilities and your experience.
**RECRUITMENT PROCESS
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