Role at a glance
- Job function
-
Supply Chain, Procurement & Trade Supply Chain Planning & Logistics
- Salary
- Not Disclosed
- Location
- China
- Employment
- Full-time
- Experience
- Clinical trial demand planning experience across design and execution
Spotted an issue?
We’ll check it against the original posting.
Role Summary
This Demand Planner role covers clinical trial demand planning across long-horizon planning, study design, and study execution. The role maintains demand assumptions and demand plans for study-level materials and works with clinical teams, supply planners, and system providers such as N-SIDE and IRT.
What You'll Do
- Input non-clinical demand into the planning system and update long-term demand in line with the defined process cadence
- Collaborate with clinical study design teams to understand high-level study design and assumptions, and incorporate demand assumptions...
- Provide robust demand scenarios and input into budget proposals for key governance decision points (DRC, E/LSPC)
- Input optimized IRT settings into IRT build and enable IRT/Supply App system integration where applicable
- Monitor demand forecast accuracy by comparing demand assumptions against actuals, escalating deviations as required
- Collaborate with Supply Planner to mitigate supply constraints and plan depot shipments to meet demand assumptions
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Clinical trial demand planner with experience across study design and execution, IRT and supply optimization tools, and senior stakeholder influence.
Required
- Clinical trial demand planning experience across design and execution
- Proven ability to translate study designs and clinical assumptions into demand plans/supply suggestions, and to re-optimise in-flight as...
- Proficiency with clinical planning/optimization tools and IRT
- Deep understanding of IRT (including configuring optimized settings) and a clinical supply optimization/scenario tool (e.g., N-SIDE...
- Track record collaborating with and influencing senior clinical and CM&S stakeholders from early design, and preparing robust...
- Digitally literate with strong analytical thinking
- Strong communication and cross-functional collaboration
Original job description
Content provided by the employer
Original job description
Content provided by the employer
Main objectives
Long Horizon Demand Planning
- Input non-clinical demand into the planning system
- Update of long-term and non-clinical demand in-line with defined process cadence
Design and Demand Planning prior to FSI
- Collaborate effectively with clinical study design teams to understand the high-level study design and assumptions
- Incorporate the demand assumptions into relevant planning systems
- Effectively communicate leverage opportunities to influence optimal design decisions with senior stakeholders and shape feasibility with clinical teams. Where applicable, leverage the N-Side Supply App to inform cost, waste and risk scenario analyses
- Provide robust demand scenarios and input into budget proposals for key governance decision points (DRC, E/LSPC)
- Input optimized IRT settings into IRT build and enable IRT/ Supply App system integration where applicable
Demand Planning during Study Execution
- Build relationships across clinical study teams to facilitate agreement of study demand and execute / challenge decision-making by communicating supply chain constraints, opportunities, and risk scenarios.
- Adhere to the planning cycle process; maintain and continuously refine demand assumptions and the demand plan for all study level materials
- Where applicable, in N-Side Supply App, use clinical assumptions and supply chain planning processes to re-optimise the study and create a supply suggestion to implement the most optimal strategy considering key KPIs (cost, waste, risk, overage). Monitor KPI’s, mitigate and escalate deviations where required
- Monitor demand forecast accuracy, by comparing demand assumptions against actuals, escalating deviation as required
- Collaborate with Supply Planner to mitigate any supply constraints
- Provide input of demand changes into the CS&OP cycle
- Plan depot shipments to meet demand assumptions with overlaid clinical intelligence
- Own re-design of the demand assumptions and plan in response to endorsed strategic change
General
- Master and apply optimization methodologies, track optimization impact on studies, and championing continuous improvement
- Work with system and service providers (e.g., N-SIDE, IRT) to manage system model and integration set up and maintenance
Education, Qualifications, Skills and Experience
1) Clinical trial demand planning experience across design and execution
· Proven ability to translate study designs and clinical assumptions into demand plans/supply suggestions, and to re-optimise in-flight as assumptions evolve.
2) Proficiency with clinical planning/optimization tools and IRT
· Deep understanding of of IRT (including configuring optimized settings) and a clinical supply optimization/scenario tool (e.g., N‑SIDE Supply App or equivalent) to assess cost, waste, risk, and overage.
3) Senior stakeholder influence and governance readiness
· Track record collaborating with and influencing senior clinical and CM&S stakeholders from early design, and preparing robust scenarios/inputs for governance decisions
4) Digitally literate and Strong analytical thinking
· ndependent use of digital tools and analytical methods to interpret information, identify meaningful insights, and make evidence-based recommendations
5) Communication and cross-functional collaboration
· Strong communication to facilitate agreement on demand, articulate constraints/trade-offs, coordinate with Supply Planning, and document decisions in planning systems.
Date Posted
28-10月-2026Closing Date
30-12月-2026AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
About the company
AstraZeneca
Large Enterprise
AstraZeneca is a global biopharmaceutical company dedicated to the research, development, and commercialization of innovative medicines. Headquartered in Cambridge, UK, the company focuses on areas such as oncology, cardiovascular, renal, metabolism, and respiratory diseases, striving to deliver life-changing treatments to patients. With a strong commitment to scientific excellence and collaboration, AstraZeneca invests in cutting-edge technologies and partnerships to drive advancements in healthcare. The company is also committed to sustainability and corporate responsibility, aiming to make a positive impact on communities worldwide.