Oncology Clinical Scientist — Phase I/II Solid Tumor

Excelya; Palaiseau; Vor Ort; EUR 70.000 - 110.000; Vollzeit

Zusammenfassung

Excelya is seeking a clinical scientist to provide scientific and clinical oversight for an ongoing Phase I/II solid tumor study. You will review patient-level safety/efficacy data, support CSR activities, and collaborate across Clinical Operations, Data Management, Statistics and CROs to ensure high-quality study execution.

The role requires strong experience in oncology development, proficiency with RECIST, and a track record in data cleaning and trial documentation.

Qualifikationen

• PharmD, PhD or equivalent in Life Sciences or related field.
• Strong experience in Clinical Development within pharma/biotech.
• Experience in Oncology Clinical Development, preferably solid tumors.
• Experience with combination therapies involving immunotherapy, targeted therapies, and/or chemo.
• Experience in clinical data review, patient-level review and data cleaning.
• Good understanding of oncology efficacy and safety endpoints like RECIST.
• Experience contributing to IB, DSUR, CSR and protocol amendments.

Aufgaben

• Provide scientific and clinical oversight of an oncology trial.
• Perform patient-level safety and efficacy data review and data cleaning.
• Support database lock preparation, study analyses and CSR activities.
• Coordinate DMC activities and centralized imaging review vendors.
• Contribute to protocol amendments, IBs, DSURs, ICFs and CSRs.
• Interpret results and support data-driven decision-making.
• Collaborate with Clinical Operations, Data Management, Statistics and CROs.

Kenntnisse

Clinical Development

Oncology

Solid Tumors

Combination Therapies

RECIST

Data Review

Study Documentation

Ausbildung

PharmD or PhD in Life Sciences

Oncology Clinical Development experience

Tools

Veeva

Clinical Databases

Jobbeschreibung

Excelya is seeking a clinical scientist to provide scientific and clinical oversight for an ongoing Phase I/II solid tumor study. You will review patient-level safety/efficacy data, support CSR activities, and collaborate across Clinical Operations, Data Management, Statistics and CROs to ensure high-quality study execution.

The role requires strong experience in oncology development, proficiency with RECIST, and a track record in data cleaning and trial documentation.