Analyst II, Trial Supply Planner
Johnson & Johnson is recruiting for an Analyst II, Trial Supply Planner to be located in Titusville, NJ; Horsham, PA or Beerse, Belgium. Remote work options may be considered on a case-by-case basis and if approved by the company.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.
We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.
At Johnson & Johnson, we all belong.
In this role you will be responsible for planning Kits for the Pack & Tech and Distribution activities of Patient dosing to meet First-Patient-In (FPI) date and consistently meet Successful Patient Dose target throughout the lifecycle of a J&J R&D trial, within budget. Generally, the focus is on large, complex studies and compounds. The Kit Supply Planning process is a key input to the Clinical Supply & Operations Planning process (cS&OP).
Key Responsibilities:
- Transition planning activities from the Clinical Supply Integrator (CSI) in the study design phase.
- Provide Master Data (MD), configure distribution networks in the relevant Kit planning systems and set planning and inventory parameters with support from the Systems and Randomization Trial Supply Management (RTSM) team.
- Set and own the trial supply budget for P&T and Distribution and work with Logistics to ensure budgets are met or adjusted in relevant systems.
- Inform CSI of budget status, risks or significant changes, including rationale.
- Adapt supply strategies (SC configuration, planning parameters) in view of changes in trial execution or protocol.
- Develop supply strategies to meet clinical plans while optimizing drug overage.
- Ensure supply planning is adapted to the latest forecast recruitment rates and inventory strategy.
- Use business tools to set and actively manage inventory targets at depots and sites and provide guidance to Trial Supply Leaders (TSL) to ensure timely delivery with minimal overage of clinical supplies.
- Responsible for transparent communications to call out any study risks via the cS&OP process.
- Identify and develop scenario analysis to drive/support decision making through the cS&OP process.
- Collaborate with the management team via Executive cS&OP, with guidance from the Team Lead.
- Attend P&T Operations meetings to ensure P&T campaigns are GMP (Good Manufacturing Practices) released by the Quality group per the order target date.
- Work independently with limited coaching, and in situations of high workload.
- Support continuous improvement initiatives.
- Responsible for managing supply and inventory issues and resolutions at the study and compound level with some guidance.
