Investigational Product Delivery Lead – Clinical Trials; m​/f​/d

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

Einsatzort: area of Basel

Art(en) der Anstellung: Temporärstelle, Vollzeit

#Lead #IP #Clinical Trials#Hands On #Cross-functional-coordination #Top Job #Your New Job

Our customer, a pharmaceutical company based in the area of Basel, needs reinforcement. For a temporary employment (duration: 01.08.2026 – 31.01.2027) we are looking for a motivated employee.

• 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

• 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

• 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

Abteilungen: Life Sciences