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Clinical Supply Chain Forecast Manager
Job in
Wrexham, Wrexham County, LL13, Wales, UK
Listed on 2026-08-10
Listing for:
Ipsen
Full Time
position Listed on 2026-08-10
Job specializations:
-
Healthcare
Healthcare Management
Job Description & How to Apply Below
Clinical Supply Chain Forecast Manager Company:
Ipsen Biopharm Ltd About Ipsen:
Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas:
Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries.
We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society!
For more information, visit us at and follow our latest news on Linked Inand Instagram.
Job Description:
WHAT
- Summary & Purpose of the Position Ipsen is a global biopharmaceutical group dedicated to improving lives and health outcomes through innovative medicines in Oncology, Neuroscience and Rare Disease.
Research and development are key elements of our strategy, reflecting our commitment to improving patients’ lives and health respect to Good Manufacturing Practices and as part of the Global Clinical Supply Management department (GCSM), the Clinical Supply Chain Forecast Managerdrive clinical supply forecasting and budgetary requirements of clinical program by providing consolidated estimates of IMPs to be produced compared to patient’s needs.
WHAT
- Main Responsibilities & Technical Competencies Clinical forecasting responsibilities
Drive clinical supply forecasting and budgetary requirements of clinical program by providing consolidated estimates of IMPs to be produced compared to patient’s needs.
Ensure adequate clinical forecast estimate / review is implemented for new / on-going clinical studies:
Organize review meetings with relevant cross functional departments
Translates into the forecasting tool the design of any new clinical study according to the study protocol as well as the recruitment projections (duration and speed of recruitment).Monitors closely the evolution of validated clinical study forecasts and shares them with the coordination, planning, packaging and distribution teams: analyzes deviations, decides on corrective actions, controls readjustments, reports on the progress of studies and validates milestones
Align with clinical manufacturing team to ensure proper planning of semi-finished goods production when required.
When clinical packaging and distribution are to be performed internally, work in tandem with clinical procurement and packaging planning manager to ensure seamless translation of the of clinical needs into production planning and take into account all the clinical studies. Main objective is on time supply to patients with no stock outs of IMP. To do so, develop, coordinate and optimize the clinical forecasts over a 3-to-12-month period
Anticipate and assess impact on changes in clinical studies managed by the GCSM team (addition of new countries, sites, number of patients, changes in protocols, etc). Propose mitigation plans for facilitating priorisation decisions. Challenge Clinical Project Managers when relevant and consolidate the new / updated forecasts in the appropriate systems. Report on the progress of studies and validate milestones
If needed, communicate, and follow up within CMC on the impact on the schedule to any changes observed or reported.
IMP estimation process:
Coordinate and lead meetings for new clinical studies (IMP kick off meeting & IMP estimation meeting) involving relevant stakeholders to ensure on time engagement of each team members.
Ensure proper IMP risk assessment is implemented and maintained for each clinical study, including but not limited to risks linked to stock out, distribution strategies, complexity of the study.
Transversal management responsibilities
Coordinate with team members in a matrix environment
Continuous improvement…
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