Specialist, RPT Production Planning and Scheduling

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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

• 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.

#LI-Remote

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite