Senior Clinical Development Scientist

Role: Supportive clinical research associate in late-stage oncology trials, focusing on CAR T-cell therapies for cancer. Responsibilities: collaborate on trial design, develop protocols and study documents, assist in data analysis and reporting, contribute to regulatory submissions, and support trial start-up, execution, and close-out activities, with potential for clinical monitoring. Requirements: PharmD or PhD in clinical research or pharmacology with relevant industry experience; MS with 6+ years; BS or RN with 8+ years in drug development, preferably in Multiple Myeloma or CAR-T therapy. Knowledge of clinical trial design, regulatory guidelines (FDA, EMA, GCP), and drug development phases is essential. Preferred: experience in oncology, immunotherapies, or cell therapies; proficiency with clinical data systems; ability to adapt to new therapeutic areas; strong communication skills; ability to travel as needed. Collaboration: work closely with Clinical Scientist Program Lead and cross-functional teams within a late-stage oncology development setting. Work setup: not specified, but involvement in multiple phases suggests a flexible, regulated environment.