Clinical Scientist

JR France; Palaiseau; Sur place; EUR 45 000 - 60 000; Plein temps

Résumé du poste

Join a leading mid-size CRO in Europe, Excelya, as a key player in Clinical Operations. You'll support oncology studies, contribute to trial documents, and collaborate with various teams to enhance the patient journey. This role offers a stimulating environment fostering personal and professional growth.

Qualifications

• Proven ability to thrive in collaborative, fast-paced environments.

Responsabilités

• Support and represent the Study Medical Manager in oncology study-related activities.
• Contribute to the development of trial-related documents.
• Perform medical review of data on patient profiles.

Connaissances

Organizational Skills

Problem-Solving

Communication

Formation

Knowledge in Immunology

Description du poste

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At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

Here’s what makes us unique

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s leading mid-size CRO with the best employee experience. Our one-stop provider service model—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey.

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.

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role offers an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical role in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities

Missions :

• Support and represent the Study Medical Manager in all oncology study-related activities from setup to closure.
• Contribute to the development of trial-related documents: abbreviated protocol, protocol, informed consent (ICF), protocol and ICF amendments, medical data validation plans, responses to medical questions, and participation in various meetings (investigators, monitors, etc.), as well as study committee preparations.
• Perform medical review of data on patient profiles, listings, and CIOMs.
• Collaborate closely with Trial Operations (TO), pharmacovigilance (CME / GSO), and statistics teams to establish listings necessary for data consistency review.
• Review study-related documents: CRF, CRF completion instructions, deviations list, validation plan, protocol review form, etc.
• Assist in reviewing interim and final study reports, associated statistical tables, and draft publications.
• Conduct medical review of files, reviews of medical listings, and contribute to the management of clinical studies (protocol writing, basic clinical analysis, study setup, medical training, medical responses) in oncology studies, regardless of study type.
• Write guidelines for medical reviews in outsourcing contexts or when applicable.

About You

At Excelya, encouraging audacious steps is a core value, so we seek individuals eager to grow with us and share our values.

• Experience: Proven ability to thrive in collaborative, fast-paced environments (we value talent over minimum years of experience!)
• Skills: Strong organizational skills, problem-solving abilities, and excellent communication skills
• Education: Knowledge in immunology is recommended
• Languages: Fluency in French and proficiency in English