Oncology Clinical Scientist - Phase I/II Data & CSR

Excelya; Saclay; On-site; EUR 65,000 - 95,000; Full time

Job summary

Excelya is seeking a skilled Clinical Scientist to lead scientific oversight in an oncology trial within Phase I/II solid tumors. You will review patient-level safety and efficacy data, contribute to data cleaning, and support CSR activities, ensuring high-quality study execution.

Requirements include a PharmD/PhD or equivalent in Life Sciences, strong oncology development experience, and fluency in English. Collaboration with CROs and cross-functional teams is essential.

Qualifications

• PharmD, PhD, or equivalent degree in Life Sciences, Biomedical Sciences, or related field.
• Strong experience in Clinical Development within pharma/biotech, especially Oncology.
• Experience with combination therapies (immunotherapy, targeted therapies, chemotherapy).
• Experience contributing to study documents (IB, DSUR, CSR).
• Experience with CROs/vendors and cross-functional teams.
• Fluent English (written and spoken).
• Experience with DMC activities or centralized imaging review is a plus.

Responsibilities

• Provide scientific and clinical oversight of an oncology trial.
• Perform patient-level safety and efficacy data review and data cleaning.
• Support database lock prep, study analyses, and CSR development.
• Coordinate DMC activities and imaging review vendors.
• Contribute to protocol amendments, IB, DSURs, ICFs, and CSRs.
• Interpret study results and support data-driven decisions.
• Collaborate with cross-functional teams to address issues.

Skills

Clinical development

Oncology

Data cleaning

RECIST

Veeva

Cross-functional

Education

PharmD or PhD or equivalent

Life Sciences/ Biomedical Sciences

Tools

Veeva

Clinical databases

Job description

Excelya is seeking a skilled Clinical Scientist to lead scientific oversight in an oncology trial within Phase I/II solid tumors. You will review patient-level safety and efficacy data, contribute to data cleaning, and support CSR activities, ensuring high-quality study execution.

Requirements include a PharmD/PhD or equivalent in Life Sciences, strong oncology development experience, and fluency in English. Collaboration with CROs and cross-functional teams is essential.