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Patient Access Program and Supply Lead

Our client is a pioneer in Drug Discovery and Development and one of the frontrunners in Personalised Healthcare. As the world`s largest R&D spender in the pharmaceutical and diagnostics domain, they work in a vast number of drug discovery & therapeutic areas and are highly recognized internationally.

We are currently looking for an enthusiastic Patient Access Program and Supply Lead for a contract of 12 months in Basel.

Main Responsibilities:

  • Actively plan and implement the Patient Access Programs (such as Pre-Approval Access & Compassionate Use programs and Post-Trial Access programs)
  • Ensure that all activities in the Community of Practice for those programs and Drug Supply are handled according to internal standards and relevant regulatory and legal compliance standards
  • Ensure adequate material and budget planning and effective delivery of Clinical Drug Supply for the conduct of managed global and local clinical trials & Patient Access Programs
  • Track and document all Patient Access Programs & supply requests
  • Facilitate and improve internal Patient Access Programs and supply processes and support shaping of Patient Access Programs’ policy
  • Liaise with, support and maintain strong relationships with all involved stakeholders and collaboration partners

Qualifications and Experience:

  • Relevant Swiss working/residency permit or Swiss/EU-Citizenship required
  • Min 5 years’ experience in pharma / clinical research (preferably in clinical trials)
  • Previous project / program management experience in pharma in international clinical trials setting
  • Excellent understanding of Health Authorities' expectations
  • Proactive and self-managed, able to adapt and flexible to an evolving matrix environment

Would you like to learn more about CTC and the opportunity outlined? Please, get in contact with us: you may either use the 'apply now' button, or write an email to us, or reach out to us on the phone.