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Investigational Product Delivery Lead – Clinical Trials (m/f/d), 100%EDP Personalberatung GmbHBasel, Basel-Stadt, Switzerland
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Investigational Product Delivery Lead – Clinical Trials (m/f/d), 100%

EDP Personalberatung GmbH
  • CH
    Basel, Basel-Stadt, Switzerland
  • CH
    Basel, Basel-Stadt, Switzerland

About

#Lead #IP #ClinicalTrials#HandsOn #Cross-functional-coordination #TopJob #YourNewJob
Our customer, a pharmaceutical company based in the area of Basel, needs reinforcement. For a temporary employment (duration: – ) we are looking for a motivated employee.

Investigational Product Delivery Lead – Clinical Trials (m/f/d), 100%

Benefits

  • An internationally operating, innovative Swiss pharmaceutical company, a leader in its field
  • Flexible working hours and extensive training opportunities
  • A motivated multicultural team and environment
  • Your 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:RobustnessAdherence to approved processesTraceability and documentationContinuous improvement
  • Proactively identify risks, gaps, and dependencies and drive resolution through direct outreac h
  • Support governance through clear reporting, visibility, and portfolio level tracking
  • Lead and facilitate monthly cross functional IP coordination meetings and contribute to portfolio reviews
  • Requirements

  • 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 TechnologyOral Solid Dosage FormsRelevant 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
  • Jetzt bewerben
    • Basel, Basel-Stadt, Switzerland

    Languages

    • English
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