About this role
Life at BMS
At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer.
Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/
The Specialist, RPT (Radiopharmaceutical Therapies) Production Planning and Scheduling will be responsible for facilitating and managing patient dose scheduling, consistent with RayzeBio corporate goals and program Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) guidelines and other applicable federal (FDA) and state regulations. The role will require significant collaboration across internal and external functions to ensure on-time delivery of patient clinical materials. This role will also ensure that such operations activities are timely, efficient, and of the highest quality.
Job Responsibilities
Essential duties and responsibilities include the following. Other duties may be assigned.
Create and maintain detailed study and site tracking for patient dosing schedules across all clinical programs
Manage and collaborate with internal and external functions for all aspects of the patient treatment schedule and dosing, including scheduling of study participant dosing, receipt and processing of drug product orders, liaison to the Clinical team on the status of drug product manufacturing, shipments and receipt
Provide support, address issues and facilitate operational continuity for the on-time delivery of patient clinical materials
Key liaison between the Clinical Site Operations, Supply Chain and Logistics, and Radiochemistry teams
Identify, mitigate, and manage closely potential risks associated with the on-time delivery of patient clinical materials and escalate accordingly to the Head of Clinical Site Operations and Head of Clinical Operations
Drive and implement continuous improvement in the planning and scheduling of patient clinical materials
Collaborate with IT Business Partners in support of modeling and scheduling simulation implementations
Maintain and update study-level clinical site procedures for RPT dose management
Performs other tasks as assigned
Leverage AI tools to enhance individual productivity and quality of work
Ability to travel approximately 10% of time
Education and Experience
Minimum 2 years of relevant experience with clinical operations, materials management and/or supply chain
BA/BS degree
Skills and Qualifications
Independent professional who proactively communicates frequently and effectively.
Organized and able to work on multiple projects with tight deadlines.
High energy level; positive attitude; works well under stress.
Hands-on, action-oriented, and able to implement effectively.
Physical Demands
While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 15 pounds. Specific vision abilities required by this job include close vision and distance vision.
Work Environment
The noise level in the work environment is usually moderate.
We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.
Compensation Overview
Remote - United States - US: $70,769 - $85,756