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.
Skills Required
- Clinical trial demand planning experience across study design and execution
- Ability to translate study designs and clinical assumptions into demand plans and supply suggestions
- Experience re-optimizing demand plans as clinical trial assumptions evolve
- Deep understanding of IRT, including configuring optimized settings
- Experience with a clinical supply optimization or scenario tool such as N-Side Supply App
- Ability to assess cost, waste, risk, and overage scenarios
- Experience influencing senior clinical and CM&S stakeholders
- Experience preparing scenarios and inputs for governance decisions
- Strong digital literacy and analytical thinking
- Strong communication and cross-functional collaboration skills
AstraZeneca Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AstraZeneca and has not been reviewed or approved by AstraZeneca.
-
Fair & Transparent Compensation — Pay is considered competitive across many roles when total rewards are factored in. Senior scientific and leadership bands are described with high ranges that reinforce competitiveness at upper levels.
-
Strong & Reliable Incentives — Bonuses, equity eligibility in many salaried roles, and solid sales on‑target earnings with upside are emphasized as meaningful parts of compensation. These elements boost overall value even where base pay is not the very highest.
-
Retirement Support — A 401(k) program with a strong company match and immediate vesting is repeatedly cited as a standout. Generous retirement support is viewed as enhancing the total package relative to peers.
AstraZeneca Insights
What We Do
We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet.







