Clinical supply chain Project Manager

Title:

Clinical supply chain Project Manager Company:

Ipsen Pharm Sciences 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 Linked Inand Instagram.

Job Description:

Job Title:

Clinical Supply Chain Project Manager Division / Function:  Pharmaceutical Development – Global Clinical Supply Manager’s

Job Title:

Clinical Supply Chain Therapeutic Area LeadWHAT
- 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 Project Managerdefines the IMP design and the associated supply chain strategy to ensure sufficient supply for clinical trialscoordinates with his / her stakeholders the set up and the maintenance of the supply chain activities related to Ipsen clinical trialsWHAT
- Main Responsibilities & Technical Competencies Project management responsibilities

Facilitate a cross functional CSC sub team, in charge of the set-up of clinical studies and which includes operational quality assurance, clinical packaging and distribution for internal projects and CDMO management for outsourced projects

Represent GCSM within clinical study team meetings and ensure seamless alignment with clinical trials milestones (timelines, study design assumptions, recruitments assumptions etc)
Define with its sub team the project and objectives while ensuring technical feasibility

Develop with its sub team comprehensive project plans to ensure on time supply to patients and avoid IMPs 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 ensure alignment 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 to meet 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 key goals ( forecasts KPIs, RTD, miss dose etc)
Present the results and progress of projects under his/her responsibility at internal / external meetings

As per delegation from the TA Lead:

Can represent GCSM in CMC project meetings and ensure adequate alignment with Asset Teams objectives (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 alignment with clinical development programs (overall plan including all studies of the program, study design assumptions etc)
IMP design and clinical supply chain definition responsibilities Propose the design of the IMP kits in partnership with…