At a Glance
- Tasks: Lead clinical supply forecasting and ensure timely delivery of medicines to patients.
- Company: Join Ipsen, a global biopharmaceutical leader focused on transformative medicines.
- Benefits: Enjoy a competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Embrace diversity and inclusion in a workplace that values your unique perspective.
- Why this job: Make a real impact on patient lives while working in a dynamic, collaborative environment.
- Qualifications: 3-5 years in pharma supply chain management and strong project management skills required.
The predicted salary is between 56700 - 69300 £ per year.
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 endeavour 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!
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 outcomes. In respect to Good Manufacturing Practices and as part of the Global Clinical Supply Management department (GCSM), the Clinical Supply Chain Forecast Manager drives clinical supply forecasting and budgetary requirements of clinical programs by providing consolidated estimates of IMPs to be produced compared to patient’s needs.
WHAT - Main Responsibilities & Technical Competencies
- Drive clinical supply forecasting and budgetary requirements of clinical programs 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.
- Translate 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).
- Monitor closely the evolution of validated clinical study forecasts and share them with the coordination, planning, packaging and distribution teams: analyse deviations, decide on corrective actions, control readjustments, report on the progress of studies and validate 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 clinical needs into production planning and take into account all the clinical studies. The main objective is on-time supply to patients with no stock outs of IMP.
- 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 prioritisation 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 member.
- 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 responsibilities: Lead change management initiatives with cross-functional teams both internally and externally to Ipsen.
- Quality: Perform activities according to Ipsen Quality Management System. Contribute to the performance of the site supporting the compliance of KPIs (First Time Quality, On time CAPA closed).
- Continuous improvement, QEHS and CSR: Contribute to continuous improvement projects within the Global Clinical Supply Management Department and/or wider Pharmaceutical Development. Be a promoter of continuous improvement processes and guarantee the method. Respect and ensure respect for applicable good practices (GMP, GMPD, etc.) and Environmental, Health and Safety rules through the procedures in force within the establishment. Drive and implement actions to develop CSR within the framework of Ipsen's orientations.
- QEEHS Responsibilities: To respect the applicable good practices (BPF, BPD, ...), the rules Energy Environment Health and Safety through the procedures in force within the establishment.
- CSR Responsibilities: To apply and make proposals within the framework of Ipsen's guidelines for actions aimed at developing CSR.
HOW - Behavioural Competencies Required
- Excellence in execution: Approaches priority setting and setting the stage through the lens of execution. Establishes clarity about the goals, accountabilities, timelines, and next steps; can identify/spot opportunities for real impact on patient and society. Able to be focused and performance-driven with clear KPIs. Plans and aligns effectively (steps, timelines etc.). Displays a commitment to best practice sharing and setting. Promotes single point of accountabilities.
- Ensures Accountability: Ensures single accountable referents per task/project/outcome (independent of organizational context or multi-team projects). Builds and anchors an environment where people have the skills and habits to ask for clarification when accountabilities are unclear. Consults/seeks relevant stakeholder views/expertise and coaches/ensures decisions are made by consent vs. consensus. Takes personal accountability for decisions, risk, actions, successes and failures, and fosters the same for others. Follows through on commitment and makes sure others do the same.
- Communicates Effectively: Asks open questions and digs deeper; shows care and respect for different perspectives (both verbally and non-verbally) and able to relate to other points of view. Communicates transparently, “tells it how it is” while keeping the communication respectful. Builds clear and crisp messages with structure and focus, uses visual communication and storytelling to make the message easy to digest and connect with the outcomes, adapted to the audience.
HOW - Knowledge & Experience
- Knowledge & Experience (essential): Approximately 3-5 years’ experience in an equivalent job within the pharmaceutical industry with significant international exposure. Experience managing complex investigational supplies for global clinical trials. Experience in project management and facilitating communications in a highly matrixed environment.
- Knowledge & Experience (preferred): Experience in using advanced supply forecasting tools including advanced use of Excel. Experience with RTSM platforms and ability to partner with external CDMOs.
- Education / Certifications (essential): Bachelor’s degree or global equivalent in pharmacy, engineering, operations and supply chain management.
- Education / Certifications (preferred): Certification in APICS, PMP, etc. Advanced education including MBA, Masters, PhD or global equivalent.
- Language(s) (essential): English.
- Language(s) (preferred): French.
We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace “The Real Us”. The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application.
Summary
Location: London (UK); Wrexham; Dublin
Type: Full time
Clinical Supply Chain Forecast Manager in Wrexham employer: Ipsen
Ipsen in Wrexham is an excellent employer, offering a collaborative work culture that prioritises innovation and excellence. Employees benefit from a supportive environment with opportunities for professional growth, all while working in a state-of-the-art packing facility that operates on a convenient Monday to Friday schedule. Join us to be part of a team that values your expertise and contributions in mechanical engineering and vision systems.
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We think this is how you could land Clinical Supply Chain Forecast Manager in Wrexham
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We think you need these skills to ace Clinical Supply Chain Forecast Manager in Wrexham
Some tips for your application 🫡
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How to prepare for a job interview at Ipsen
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Ipsen that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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