Offre d'emploi : Clinical Biomarker Manager

Gosselies, Charleroi
mardi 19 mai 2020
Date limite
vendredi 3 juillet 2020
Type de contrat
Temps de travail
Temps plein

iTeos Therapeutics is a privately-held, clinical-stage biopharmaceutical company dedicated to extending and improving the lives of cancer patients by designing and developing next generation immunotherapies. iTeos Therapeutics is advancing its two main programs into a phase I/II clinical stage. The first program is an insurmountable and non-brain penetrant adenosine A2A receptor antagonist. The second program is a human ADCC-enabling anti-TIGIT antibody.

Based in Gosselies, Belgium and Cambridge, 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 led by 6 main US Venture Capitalists. All previous investors including Fund +, VIVES II and SRIW, as well as SFPI, also participated in this funding round. For more information, please visit

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 (m/f) :

Clinical Biomarker Manager

Main responsibilities:

Within its Translational Medicine department, iTeos is currently actively looking for a highly motivated Scientist to coordinate the preparation, implementation, follow-up and interpretation of results of biological analyses (ie PK, PD and biomarkers) in clinical trials in close interaction with Translational Medicine Scientists, Clinical Trial Managers, Medical Directors and CROs. The successful candidate will be an autonomous, proactive, collaborative scientist with experience working in a clinical development environment.

More specifically, the responsibilities will be to :

  • Contribute to the preparation of biological analyses in clinical trials by :
    • participating to the selection of analytical and central laboratories (including service providers, and/or commercial partners),
    • managing contracts with the support of a Legal Advisor,
    • planning and following-up the activities related to the implementation of biological analyses in clinical trials (e.g. assay transfer, kit preparation, sample collection procedures, shipping requirements, CRF review, analytical data collection/reporting and data transfer) with different service providers.
  • Follow-up and monitor the activities related to biological analyses during ongoing clinical trials (including coordination with the central lab and the other laboratories, follow-up of samples), identify study or project issues and solve them. Contribute to the preparation of the budget related to these activities as well as its follow-up.
  • Collaborate on the transfer, review, analysis, and interpretation of the corresponding results and assure appropriate data review and accurate data reporting.
  • Support the development of dedicated sections of interim analysis and study report.
  • Contribute to presentations and communications of study data results internally and to external audiences including investigators at sponsor meetings or general audiences at scientific conferences.
  • Conduct literature reviews as needed for study rational, and the interpretation of study data and development of next steps.


  • You hold a Master degree, PhD or PharmD in Life Sciences.
  • You have at least 5 years’ experience in organizing, implementing and monitoring analysis of biological markers during clinical trials, ideally in immuno-oncology. An experience in the follow-up of contractual aspects and relations is an advantage. A previous experience in laboratory is important to be able to coordinate experiments in clinical settings
  • You have a good understanding of GCP/GCLP guidelines and current global regulations
  • You have a good understanding of trial design and statistics
  • You master Standard Office tools (knowledge in MS project is an asset), as well as data analysis software (eg xls, Prism, Jump) 
  • You are fluent in French and English (oral and written).
  • You have strong problem-solving skills.
  • Strongly organized and rigorous, you have a good ability to adapt to changes in priorities and to work effectively on multiple programs in a fast-paced environment.
  • Although autonomous, you have a high ability to collaborate with internal and external stakeholders.
  • You are very open-minded and have excellent interpersonal and communication skills.
  • Since the job scope/role could evolve as the company grows, you are flexible in terms of responsibilities, in alignment with your profile. 


  • A stimulating scientific position within a high-potential innovative biotech company.
  • The opportunity to work in a science-driven, dynamic, human‐sized, respectful and professional environment.
  • A challenging scientific and business growth in which you get to bring your knowledge and skills.
  • Varied contacts inside the company, the biotech/pharma sector and the scientific world.
  • A long-term contract and an attractive salary package in line with the position responsibilities and your experience.

 Interested ?

Send your CV together with an adapted cover letter via or to the following address :

Your application and related information will remain strictly confidential.

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