Specialist, RPT Production Planning and Scheduling

Role: Radiopharmaceutical Therapies (RPT) Production Planning and Scheduling Specialist responsible for managing patient dose scheduling in clinical programs, ensuring compliance with GCP/ICH, FDA, and other regulations. Responsibilities include creating and maintaining study/site tracking, coordinating with internal teams and external partners on dosing schedules, drug manufacturing, and logistics, and facilitating operational continuity for timely delivery of clinical materials. The role emphasizes risk mitigation, process improvement, and leveraging AI tools to enhance productivity. Requirements: BA/BS degree with at least 2 years experience in clinical operations, supply chain, or materials management; proactive communication skills; organized, detail-oriented, and able to handle multiple projects under tight deadlines. Preferred skills include experience with radiopharmaceuticals, clinical trial operations, and cross-functional collaboration. High-value biopharma specifics: involvement in radiopharmaceutical therapies for cancer, supporting clinical trial logistics, with approximately 10% travel. Work setup: remote in the U.S., with responsibilities aligned to clinical development stages and regulatory compliance.