Project Research Scientist

JR France; Palaiseau; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading company in healthcare is seeking a professional to support oncology studies. The role involves collaborating with various teams, contributing to trial documentation, and performing medical reviews. Fluency in French and English is required.

Qualifications

• Experience in oncology research and clinical studies.
• Ability to contribute to trial documents and medical reviews.

Responsabilités

• Support Study Medical Manager in oncology study activities.
• Contribute to trial documents and medical reviews.
• Collaborate with Trial Operations and pharmacovigilance teams.

Connaissances

Fluency in French

Good level of English

Description du poste

Client:

Excelya

Location:

Not specified

Job Category:

Other

EU work permit required:

Yes

Job Reference:

98342483363312435232760

Job Views:

3

Posted:

15.05.2025

Expiry Date:

29.06.2025

Job Description:

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare. Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.

You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Responsibilities include:

1. Supporting and representing the Study Medical Manager in all oncology study-related activities from setup to closure.
2. Contributing to the development of trial documents: abbreviated protocols, protocols, informed consent forms (ICF), amendments, medical data validation plans, and responses to medical questions.
3. Participating in various meetings (investigators, monitors, etc.) and conducting medical reviews of patient data, listings, and CIOMs.
4. Collaborating closely with Trial Operations, pharmacovigilance, and statistics teams for data review and consistency.
5. Reviewing interim and final study reports, statistical tables, and assisting with draft publications.
6. Performing medical review of files, listings, and managing clinical studies, including protocol writing, clinical analysis, setup, training, and medical responses in oncology research.
7. Writing guidelines for medical reviews, especially in outsourcing contexts.

Fluency in French and a good level of English are required.

Please note that if you are not a passport holder of the country for the vacancy, you might need a work permit. Check our Blog for more information.

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