Specialist, RPT Production Planning and Scheduling

Bristol Myers Squibb; United States; On-site; USD 90,000 - 140,000; Full time

Job summary

Scorpion Therapeutics is seeking a Radiopharmaceutical Therapies (RPT) Production Planning and Scheduling Specialist to manage patient dose scheduling in clinical programs, ensuring compliance with GCP/ICH, FDA, and other regulations.

You will create and maintain study/site tracking, coordinate with internal teams and external partners on dosing schedules, drug manufacturing and logistics, and facilitate ongoing operations to deliver clinical materials on time.

Qualifications

• BA/BS degree with at least 2 years experience in clinical operations, supply chain, or materials management.
• Proactive communication skills; organized and detail-oriented; able to handle multiple projects under tight deadlines.

Responsibilities

• Manage patient dose scheduling in clinical programs.
• Create and maintain study/site tracking across trials.
• Coordinate with internal teams and external partners on dosing schedules, drug manufacturing, and logistics.
• Facilitate operational continuity to ensure timely delivery of clinical materials.
• Focus on risk mitigation, process improvement, and leveraging AI tools to boost productivity.

Skills

Proactive communication

Organized & detail-oriented

Multitasking under tight deadlines

Education

BA/BS degree

Job description

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

• experience with radiopharmaceuticals
• clinical trial operations
• 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.