In this role, you will manage and oversee clinical trial activities across all study phases within Switzerland, ensuring high-quality execution and regulatory compliance. You will play a key role in site management, monitoring, and coordination between stakeholders. The position requires a strong operational mindset and the ability to drive studies efficiently from initiation through close-out.

Start Date: 01.06.2026

Duration: Permanent Position

Place of Work: Neuchâtel

Key Responsibilities

  • Support the planning, coordination, and execution of clinical trials throughout all phases of the study lifecycle
  • Contribute to feasibility assessments, site identification, and start-up activities including regulatory and ethics submissions
  • Conduct on-site monitoring visits such as site initiation, routine monitoring, and close-out visits
  • Ensure that clinical trials are conducted in compliance with study protocols, ICH-GCP guidelines, and applicable regulations
  • Review and verify clinical data, source documents, and study records to ensure accuracy and completeness
  • Prepare and maintain essential clinical documentation including monitoring reports and study-related correspondence
  • Build and maintain strong relationships with investigational sites and external stakeholders
  • Identify, track, and follow up on study-related issues, deviations, and corrective actions
  • Coordinate site activities and support operational aspects of site management, including contracts and timelines
  • Act as a key liaison between study sites, sponsors, and internal teams
  • Support the preparation and submission of regulatory documentation and study updates where required
  • Contribute to process improvements and ensure efficient study execution

Candidate Profile

  • Degree in Life Sciences, Pharmacy, or a related discipline
  • Extensive experience in clinical research, including several years in a CRA or similar role
  • Strong knowledge of ICH-GCP and applicable clinical trial regulations
  • Familiarity with the Swiss clinical research environment and site landscape
  • Experience in monitoring clinical trials across multiple phases
  • Strong documentation skills with attention to detail and quality standards
  • Ability to manage multiple priorities and work independently
  • Excellent communication and stakeholder management skills
  • Fluent in English, French, and German

 

 

 

 

 

Job ID 18870