Biomarker Operations Manager

il y a 1 semaine


Gosselies, Belgique iTeos Therapeutics Temps plein

**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.

Our values - Data Driven, Ownership, Courage, and Stronger Together - form the foundation of who we are as a company and define who we are at our core.

**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 Biomarker Operations Manager.**

**ROLE: Biomarker Operations Manager**

**MAIN RESPONSIBILITIES**
- Contribute to the preparation of biological analyses in clinical trials by
- participating to the selection of analytical 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 and analysis of the corresponding results and ensure appropriate data review and accurate data reporting.
- Support the development of dedicated sections of interim analysis and study report.

**PROFESSIONAL EXPERIENCE/QUALIFICATIONS**
- You hold a Bachelor or Master degree in Life Sciences or PharmD.
- Experience in oncology/immuno-oncology is an advantage.
- Prior experience in a laboratory environment is important to be able to coordinate experiments in clinical settings.
- Experience in the follow-up of contractual aspects and relations is an advantage.
- You have strong problem-solving skills.
- You are open-minded and have excellent interpersonal and communication skills.
- You have a good understanding of GCP/GCLP guidelines and current global regulations.
- You are fluent in French and English (oral and written).
- Well organized and resilient, you are able to adapt to changes in priorities and to work effectively on multiple programs in a fast-paced environment.
- Although largely autonomous, you are collaborative and are happy to work with internal and external stakeholders.
- You master Standard Office tools (knowledge in MS project is an asset.
- Since the job scope/role could evolve as the company grows, you can adapt to changing needs.

**OFFER**
- A stimulating position within a high-potential innovative biotech company.
- The opportunity to work in a science-driven, dynamic, respectful, and professional environment.
- A challenging scientific and business growth in which you get to bring your knowledge and skills.
- An employment agreement contract with an attractive salary package in line with the position responsibilities and your experience.

**RECRUITMENT PROCESS


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