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• Understand scientific, strategic, and safety considerations in clinical trial design.
• Develop budgets and plan resources effectively for clinical trials.
• Select appropriate investigator sites for trial implementation.
• Identify the role of Contract Research Organisations (CROs) and external providers in clinical trial management.
• Familiarise with essential clinical trial documents and their significance in trial conduct.
• Navigate the submission process to Swiss Ethics Committees (EC) and Regulatory Authorities (RA).
• Implement risk management strategies to ensure trial safety and compliance.

• Proficiency in designing clinical trials considering scientific, strategic, and safety aspects.
• Ability to develop and manage budgets for clinical trial operations.
• Skill in selecting investigator sites based on strategic criteria and operational feasibility.
• Understanding of the roles and responsibilities of CROs and external providers in clinical trial management.
• Competence in preparing and managing essential clinical trial documents.
• Proficiency in navigating the submission process to Swiss Ethics Committees and Regulatory Authorities.
• Ability to implement risk management strategies to mitigate potential risks during trial conduct.

CHF 1,800

a) Holders of a university master's degree or doctorate in science, medicine or pharmacy or a qualification deemed equivalent;
or a bachelor's degree in nursing from a Swiss ÓñÃÀÈË´«Ã½ of Applied Sciences;
or a qualification deemed equivalent or professional experience deemed equivalent by the programme directors.

b) Good oral and written comprehension of English (equivalent to level B2-C1)

• Copy of identity document
• Curriculum Vitae
• Copies of relevant university degrees
• Covering letter

• Dr Shelly BUSTION
• Dr Sandrine CHARVAT