Clinical Scientist Oncology

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

This role offers an exciting opportunity to join an Oncology Clinical Science team supporting an ongoing Phase I/II solid tumor clinical study evaluating targeted therapies, immunotherapies, and chemotherapy combinations. You will provide scientific oversight, contribute to patient-level data review, support study deliverables through database lock and Clinical Study Report (CSR) activities, and collaborate with cross-functional teams to ensure high-quality study execution.

• →Support the Clinical Lead and Study Team in the scientific and clinical oversight of an oncology clinical trial.
• →Perform patient-level review of safety and efficacy data and contribute to data cleaning activities.
• →Support database lock preparation, study analyses, and CSR development.
• →Coordinate Data Monitoring Committee (DMC) activities and centralized imaging review vendors.
• →Contribute to key clinical documents including protocol amendments, Investigator's Brochure (IB), DSURs, ICFs, and CSRs.
• →Interpret study results and support data-driven decision-making.
• →Collaborate with Clinical Operations, Data Management, Statistics, Safety, CROs, and investigational sites.
• →Identify and proactively address study, data, or operational issues.
• →Ensure all activities are conducted in compliance with ICH-GCP and applicable regulations.

• 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.
• Experience with combination therapies involving immunotherapy, targeted therapies, and/or chemotherapy.
• Experience in clinical data review, patient-level review, and data cleaning.
• Good understanding of oncology efficacy and safety endpoints, including RECIST assessments.
• Experience contributing to clinical study documents (IB, DSUR, protocol amendments, CSR).
• Experience working with CROs, vendors, and cross-functional study teams.
• Experience with DMC activities or centralized imaging review is a plus.
• Fluent English (written and spoken).
• Experience with Veeva and clinical databases/listings is desirable.