Oncology Clinical Scientist – Phase I/II (Solid Tumors)

Excelya Group; Saclay; Presencial; EUR 65.000 - 95.000; Jornada completa

Descripción de la vacante

Excelya is seeking a scientifically rigorous professional to join our Oncology Clinical Science team in France. The role focuses on supporting an ongoing Phase I/II solid tumor study with targeted and combination therapies, contributing to data review, CSR activities, and cross-functional collaboration to ensure high-quality study execution.

You will oversee patient-level data review, support database lock, and contribute to study deliverables while maintaining compliance with ICH-GCP.

Formación

• PharmD, PhD, or equivalent degree in Life Sciences, Biomedical Sciences, or a related field.
• Strong experience in Clinical Development within the pharmaceutical or biotechnology industry.
• Experience in Oncology Clinical Development, preferably in solid tumors.

Responsabilidades

• Provide scientific and clinical oversight of an oncology trial.
• Perform patient-level safety and efficacy data reviews and data cleaning contributions.
• Support database lock, study analyses, and CSR development.
• Coordinate DMC activities and centralized imaging review vendors.
• Contribute to protocol amendments, IB, DSURs, and CSRs.
• Interpret study results and support data-driven decisions.
• Collaborate with Clinical Operations, Data Management, Statistics, Safety, CROs, and sites.
• Identify and address study, data, or operational issues.
• Ensure activities comply with ICH-GCP and regulations.

Conocimientos

Clinical Development

Oncology

Data Review

RECIST

Cross-functional Collaboration

Educación

PharmD/PhD or equivalent

Herramientas

Veeva

Clinical Databases

Descripción del empleo

Excelya is seeking a scientifically rigorous professional to join our Oncology Clinical Science team in France. The role focuses on supporting an ongoing Phase I/II solid tumor study with targeted and combination therapies, contributing to data review, CSR activities, and cross-functional collaboration to ensure high-quality study execution.

You will oversee patient-level data review, support database lock, and contribute to study deliverables while maintaining compliance with ICH-GCP.