Das ist der Job
The company is a fast-paced biotech with a collaborative culture, committed to continuous innovation in cell therapy.
Darum lohnt es sich
Qualifications:
• Master's degree in a quantitative field with 5+ years experience, or bachelor's with 8+ years.
• Strong proficiency in SAS and/or R for clinical trial data analysis.
• Working knowledge of CDISC standards and regulatory submission requirements.
• This role operates in a professional office or remote work environment.
• Employees are expected to maintain a safe, distraction-free workspace.
• Remote collaboration with biostatisticians, data managers, and clinical teams. • Develop, validate, and maintain SAS and/or R programs for SDTM, ADaM datasets, and TLFs.
• Support statistical analyses for safety reports, publications, and regulatory submissions.
• Ensure compliance with FDA 21 CFR Part 11, GxP, and internal SOPs.
Iovance Biotherapeutics
Iovance Biotherapeutics is a global leader in innovating, developing, and delivering tumor infiltrating lymphocyte (TIL) therapy for cancer.
