Clinical Supply Chain Project Manager

Ipsen

  • Dreux, Eure-et-Loir
  • CDI
  • Temps-plein
  • Il y a 29 jours
Title: Clinical Supply Chain Project ManagerCompany: Ipsen PharmSciences SASAbout 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 and .Job Description:Summary / purpose of the positionIpsen is a global biopharmaceutical group dedicated to improving lives and health outcomes through innovativemedicines in Oncology, Neuroscience and Rare Disease. We are committed to discovering new treatments in areaswith high unmet medical needs and improving the quality of life for patients.Research and development are key elements of our strategy, reflecting our commitment to improving patients’lives and health outcomes. Bolstered by a culture of collaboration & excellence, Ipsen offers a unique propositionto 5,700+ employees committed to society.The Pharmaceutical Development organization is located across 4 Sites (France, Ireland, UK and Canada). Theposition is located in France, dedicated to the development of small molecules, peptides and devices.In respect to Good Manufacturing Practices and as part of the Global Clinical Supply Management department(GCSM), the clinical supply chain project manager
  • defines the IMP design and the associated supply chain strategy to ensure sufficient supply for clinical
trials
  • coordinates with his / her stakeholders the set up and the maintenance of the supply chain plan related
to Ipsen clinical trialsThis entails to be strongly involved in the continuous improvement process and knowledge management relatingto the development of NCEs and Life cycle management of commercial products within the DPD department.Main responsibilities / job expectationsProject management responsibilities- Facilitate a cross functional CMC sub team, in charge of the set-up of clinical studies and which includesoperational quality assurance, clinical packaging and distribution for internal projects and CDMOmanagement for outsourced projects- Represent GCSM within clinical study team meetings and ensure seamless alignment with clinical trialsmilestones (timelines, study design assumptions, recruitments assumptions etc)- Define with its sub team the project scope and objectives while ensuring technical feasibility- Develop with its sub team comprehensive project plans to ensure on time supply to patients and avoidIMPs stock out- Validate the strategy with the Clinical Supply Chain Therapeutic Area Lead- Develop strong collaboration with Global Regulatory Affairs and CMC Regulatory teams to ensurealignment of regulatory strategy (submission filing, product references to be used)- Evaluate impact of changes to the project scope, project schedule, and project costs- Facilitate the sub team to solve complex challenges and provide mitigation plans in a timely manner tomeet the business needs- Escalate challenges / issues to management when needed- Measure performance using appropriate project management tools and techniques- Initiate and maintain risk assessment to minimize supply chain potential risks- Track project performance, specifically to analyze the successful completion of short and long-term keygoals (OTIF, forecasts KPIs, RFT etc)- Present the results and progress of projects under his/her responsibility at internal / external meetings- As per delegation from the Supply Chain TA Lead:- Can represent GCSM in CMC project meetings and ensure adequate alignment with Asset Teamsobjectives (timelines, priorities, need to initiate / review forecasts, communication escalation,anticipate risks and provide mitigation)- Can represent GCSM within Clinical Operations strategic meetings and ensure seamless alignmentwith clinical development programs (overall plan including all studies of the program, study designassumptions etc)IMP design and clinical supply chain definition responsibilities- Propose the design of the IMP kits in partnership with packaging team or CDMO- Manage the labelling definition and approval- Create and maintain comprehensive project documentation (IMP Design and Supply / Handling Manual /Supply Chain Flow Diagram, leaflets)- Review Clinical Operations documentation (CRO scope of work for example)- Define with the Forecast Manager the initial needs to support clinical trials- Ensure all studies forecasts are revisited on a regular basis with the support of the Forecast Managerwhen needed:- Organize review meetings with relevant cross functional departments- Monitor closely the evolution of validated clinical study forecasts and share them with the CMC subteam- Anticipate and assess impacts on changes on its clinical studies (addition of new countries, sites,number of patients, changes in protocols, etc). Challenge Clinical Project Managers when relevantand consolidate the new / updated forecasts in the appropriate systems.- Report on the progress of studies and validate milestones- Perform his / her mission according to (i) the up-to-date internal and external regulatory guidance andprocess, (ii) and harmonized ways of working / processes as defined by the Portfolio Management andProcesses Team- Manage quality events (deviations, change controls) in line with defined KPIs,Continuous improvement responsibilities- Support the Process and Compliance Project Manager while defining and / or adjusting GCSM processes /ways of working and providing effective as well as continuous feedback.- Organize and actively participate in lessons learnt exercises when needed.- Contribute to continuous improvement projects within the Global Clinical Supply Management Departmentand/or wider Pharmaceutical Development.- Be a promoter of continuous improvement processes and to guarantee the method.QEEHS Responsibilities responsibilities- Respect the Good Practices applicable (BPF, BPD, …), the rules of Energy Environment Health and Safetythrough the procedures applicable within the company.CSR Responsibilities:- Apply and proactively contribute to actions for CSR development according to Ipsen guidelines.Knowledge, abilities & experienceEducation / Certifications:
  • Pharmacist, engineer or university graduate (BAC+5) with a postgraduate degree in "health industry"
Experience:
  • Minimum 5 experience in an equivalent job in the Pharmaceutical Industry with a significant
international exposureLanguages:
  • Proficient in French and English
Key Technical Competencies Required- Experience and knowledge on handling large and complex clinical trials (preferred)- Good communication skills / networking- Experience in project management- Team player with ability to work in a matrix and global environment- Strong organizational skillsHybrid model : 3 days on site & 2 days on remoteDans le cadre de ses recrutements IPSEN s’engage au respect de l’égalité de traitement des candidats, indépendamment du sexe, de l’âge, de l'orientation sexuelle, de l'origine ethnique, de la couleur de la peau, de la nationalité, du handicap ou de l'appartenance à un syndicat.

Ipsen