PpEquivalent annual salary range : 115 K to 122 K CHF /ppWe are seeking an experienced Investigational Product Delivery Lead to join a dynamic Health, Nutrition Care organization and play a key role in supporting clinical development programs /pp.In this position, you will act as the central coordination point for investigational product activities across multiple clinical studies, ensuring seamless collaboration between scientific, operational, technical, and external stakeholders /ph3Your Responsibilities /h3ulliCoordinate investigational product delivery activities across a portfolio of clinical trials from planning through execution. /liliServe as the primary liaison between Clinical Operations, Clinical Trial Management, Quality, Manufacturing, Supply Chain, Analytics, technical teams, and external partners. /liliDrive alignment across functions to ensure milestones, quality expectations, and regulatory requirements are consistently met. /liliTranslate clinical and operational requirements into actionable deliverables for technical and manufacturing teams. /liliMaintain clear communication across stakeholders and proactively manage changes, timelines, and dependencies. /liliEnsure compliance with investigational product processes, documentation standards, traceability requirements, and quality expectations. /liliIdentify and mitigate risks, bottlenecks, and execution gaps through proactive stakeholder engagement. /liliFacilitate cross-functional governance meetings, provide portfolio visibility, and contribute to strategic planning and review activities. /li /ulh3Your Profile /h3ulliDegree in Pharmacy, Pharmaceutical Sciences, Chemistry, Chemical Engineering, Materials Science, or a related scientific field. /lili3–5 years of experience within pharmaceutical, nutraceutical, dietary supplement, or clinical development environments. /liliStrong knowledge of product development and manufacturing processes, ideally from concept through commercialization. /liliHands‑on experience in Quality, Pharmaceutical Technology, Oral Solid Dosage Forms, or related areas. /liliFamiliarity with GMP requirements, Pharmacopeia standards, and relevant regulatory frameworks. /liliGood understanding of clinical trial processes and investigational product management. /liliExperience working with CTMS, Veeva, or similar clinical systems. /liliPractical project coordination and stakeholder management skills with the ability to work effectively across multiple functions. /liliKnowledge of materials science and chemical sciences would be considered a strong advantage. /li /ulh3What You'll Bring /h3ulliStrong organizational and communication skills. /liliA proactive, solution‑oriented mindset. /liliThe ability to manage multiple priorities in a fast‑paced environment. /liliExperience driving process execution, monitoring performance, and reporting progress to stakeholders. /li /ul /p #J-18808-Ljbffr