Clinical Trial Assistant
il y a 2 semaines
**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 Trial Assistant.**
**ROLE: Clinical Trial Assistant**
**MAIN RESPONSIBILITIES**
- To provide general administrative support to the Clinical Operations Department and assistance to Clinical Study Manager(s) and Site Manager(s).
- Assist in the formatting, editing and processing of essential clinical study documents (protocols, IB, reports, ICFs, etc).
- Assist Study Managers with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Support in translation/back translation of trial documents, and documents for internal and/or external use.
- Responsible for the correct filing and archiving of clinical study documents, and the maintenance of study files (TMF). Ensure that all documents can be traced at any time for internal and external use and/or audits.
- Provides support in meeting activities such as organizing and planning of meetings (e.g.study, team
- meetings), and provide meeting minutes.
- Contribute to the optimization of processes, and development of study specific tools within the Clinical Operations department.
- To assist in quality control audits of clinical study documentation (e.g. Main Study Files, etc.).
- To assist with the coordination of team member tracking and study specific trainings.
- To assist in the tracking and distribution of safety reports.
- Support in clinical trial payment process.
**PROFESSIONAL EXPERIENCE/QUALIFICATIONS**
- Written and spoken fluency in English and French
- Excellent computer skills - MS office
- Communication and organization skills
- Very high accuracy
- Flexibility and hands-on initiative
- Sense of responsibility
- Basic knowledge of medical terminology is an asset
- Capacity to work autonomously and in a team
- Eager to learn
**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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