Equivalent annual salary range : 115 K to 122 K CHF
We 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
.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
Your Responsibilities
* Coordinate investigational product delivery activities across a portfolio of clinical trials from planning through execution.
* Serve as the primary liaison between Clinical Operations, Clinical Trial Management, Quality, Manufacturing, Supply Chain, Analytics, technical teams, and external partners.
* Drive alignment across functions to ensure milestones, quality expectations, and regulatory requirements are consistently met.
* Translate clinical and operational requirements into actionable deliverables for technical and manufacturing teams.
* Maintain clear communication across stakeholders and proactively manage changes, timelines, and dependencies.
* Ensure compliance with investigational product processes, documentation standards, traceability requirements, and quality expectations.
* Identify and mitigate risks, bottlenecks, and execution gaps through proactive stakeholder engagement.
* Facilitate cross-functional governance meetings, provide portfolio visibility, and contribute to strategic planning and review activities.
Your Profile
* Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Chemical Engineering, Materials Science, or a related scientific field.
* 3–5 years of experience within pharmaceutical, nutraceutical, dietary supplement, or clinical development environments.
* Strong knowledge of product development and manufacturing processes, ideally from concept through commercialization.
* Hands‑on experience in Quality, Pharmaceutical Technology, Oral Solid Dosage Forms, or related areas.
* Familiarity with GMP requirements, Pharmacopeia standards, and relevant regulatory frameworks.
* Good understanding of clinical trial processes and investigational product management.
* Experience working with CTMS, Veeva, or similar clinical systems.
* Practical project coordination and stakeholder management skills with the ability to work effectively across multiple functions.
* Knowledge of materials science and chemical sciences would be considered a strong advantage.
What You'll Bring
* Strong organizational and communication skills.
* A proactive, solution‑oriented mindset.
* The ability to manage multiple priorities in a fast‑paced environment.
* Experience driving process execution, monitoring performance, and reporting progress to stakeholders.
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