Clinical Supply Chain Project Manager
Ipsen
full-time
Posted on:
Location Type: Hybrid
Location: Dreux • France
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About the role
- Facilitate a cross functional CMC 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)
- Develop strong collaboration with Global Regulatory Affairs and CMC Regulatory teams to ensure alignment of regulatory strategy (submission filing, product references to be used)
- 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 (OTIF, forecasts KPIs, RFT etc)
Requirements
- Minimum 5 experience in an equivalent job in the Pharmaceutical Industry with a significant international exposure
- Pharmacist, engineer or university graduate (BAC+5) with a postgraduate degree in "health industry"
- Proficient in French and English
- Experience and knowledge on handling large and complex clinical trials (preferred)
- Good communication skills / networking
- Experience in project management
- Strong organizational skills
Benefits
- Flexible work arrangements
- Professional development
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
project managementrisk assessmentclinical trialsregulatory strategysupply chain managementoperational quality assuranceclinical packagingdistribution
Soft skills
communication skillscollaborationorganizational skillsnetworking
Certifications
Pharmacistengineeruniversity graduatepostgraduate degree in health industry