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Investigational Product Delivery Lead

Job in 4303, Kaiseraugst, Kanton Aargau, Switzerland
Listing for: Experis Schweiz
Full Time position
Listed on 2026-06-21
Job specializations:
  • Pharmaceutical
Salary/Wage Range or Industry Benchmark: 100000 - 125000 CHF Yearly CHF 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Location: Kaiseraugst

We are looking for an Investigational Product Delivery Lead for one of our main clients in Kaiseraugst.

Key Responsibilities
  • Coordinate end‑to‑end investigational product delivery across 5–10 active clinical trials
  • Act as the single coordination point between various stakeholders, Clinical Trials Management, Clinical Operations, technical teams, Quality, Manufacturing, Supply Chain, Analytics, and external partners
  • Actively engage and follow up with functions to ensure execution against timelines, quality, and regulatory requirements
  • Maintain constant, structured communication with technical teams to translate clinical needs into executable technical actions, and keep all functions involved well informed and aware about changes in timelines
  • Ensure consistent application of the IP process with focus on:
    • Robustness
    • Adherence to approved processes
    • Traceability and documentation
    • Continuous improvement
  • Proactively identify risks, gaps, and dependencies and drive resolution through direct outreach
  • Support governance through clear reporting, visibility, and portfolio‑level tracking
  • Lead and facilitate monthly cross‑functional IP coordination meetings and contribute to portfolio reviews
Qualifications
  • Degree in Pharmacy, Pharmaceutical Sciences, Chemical Engineering, Materials Science, Chemistry, or a related scientific discipline
  • Good understanding on dietary supplement product development and manufacturing procedure from idea to product
  • 3–5 years hands‑on experience in:
    • Quality and/or Pharmaceutical Technology
    • Oral Solid Dosage Forms
    • Relevant regulatory frameworks (e.g. Pharmacopeia, GMP)
    • Dietary supplement experience
  • Solid understanding of clinical trial workflows
  • Experience with CTMS, Veeva, or equivalent clinical systems
  • Basic but practical project management capability
  • A strong understanding of materials and chemical sciences is considered an asset
  • Process deployment, execution monitoring, and reporting
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