Job Information
Bristol Myers Squibb Specialist, RPT Production Planning and Scheduling in United States
Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .
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 at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
Company: Bristol-Myers Squibb
Req Number: R1583383
Updated: 2024-08-19 03:27:31.907 UTC
Location: Field-
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
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