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Investigational Product Delivery Lead  

Sede

Svizzera, Basilea Città, Kaiseraugst

Settore:

Industria farmaceutica

Ruolo:

Risorse umane

Data ultimo aggiornamento: 04/06/2026

attività 

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



Description:

Key Responsibilities (6-8 bullet points):

  • 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


You bring (6-8 bullet points):
·

  • 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

Contact: alba Jansa: alba.jansa@experis.ch
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