Global Planer CTS Supply Chain at CSL Behring
3MADL, Hessen, Germany -
Full Time


Start Date

Immediate

Expiry Date

04 Aug, 25

Salary

0.0

Posted On

26 Mar, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Research, Supply Management, Life Sciences, Regulations, Pharmaceutical Industry

Industry

Pharmaceuticals

Description

For our Clinical Trial Supply department, in Marburg, Bern, Zürich or King of Prussia, we are looking for a
Global Planner, Clinical Trial Supply (m/f/x)
R-251735
Fulltime / permanent / tariff
Internal job title: Global Planner CTS Supply Chain
Internal closing date: 08.04.2025

The Opportunity

  • Responsible for efficient, cost-effective clinical trial supply planning and management for low complexity studies
  • Performs planning and forecasting of drug volume requirements sample collection, analysis and ensures proper storage, transportation and archiving
  • Assists with selection and management of external service providers in compliance with outsourcing strategy to assure cost efficient and high quality services
  • Leverages CSL’s interactive response technology (IRT) system to support clinical supply management activities
  • Authors/reviews critical study documents (e.g. study protocol, product dossiers, handling instructions, study reports)
  • Leads or participates in global CTS project meetings with internal and external team members
  • Partners with R&D and other functions to ensure optimal use of systems and processes to support clinical trial supply chain
  • Supports continuous improvements in clinical drug supply and revises SOPs to ensure ongoing compliance and efficient conduct of clinical trial supply activities

Your Skills and Experience

  • University degree (BSc, MSc) in life sciences, engineering, logistics or equivalent experience
  • 5+ years’ experience in clinical research and/or clinical supply management or global R&D project management in the pharmaceutical industry
  • Knowledge of ICH-GCP regulations and the conduct of clinical studies
  • Knowledge of cGMP and cGDP regulations

What we offer

  • Hybrid working models.
  • Learning opportunities with our CSL Academy.
  • Global and diverse environment with modern workspaces.
  • Up to two additional leave days for your personal wellbeing.

For more information, please check out our global benefits below
We are looking forward to your application. Please ensure to apply online with your CV and certifications as well as your salary expectation.
applicable.

Responsibilities

Please refer the Job description for details

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