(Senior) Clinical Trial Monitor

Tasks

• Responsible for the quality control of clinical trials phase I to IV, both nationally and internationally
• Ensure study sites conduct clinical trials in accordance with the protocol, ICH-GCP guidelines, and the applicable regulations
• Perform on site and remote monitoring activities from study initiation to study completion
• Conduct central data monitoring
• Identify, assess, and resolve any site-related issues to ensure smooth trial progress and maintain high data quality
• Document monitoring activities thoroughly, including monitoring reports, protocol deviations, and action items to be addressed
• Collaborate with study teams, investigators, and sponsors to address trial-related concerns and optimize patient safety and trial performance
• Review and evaluate trial data to detect trends, discrepancies, and potential issues
• Perform investigational product (IP) inventory, reconciliation and review storage and security
• Additional responsibilities : Provide training and lectures for various courses related to clinical research

Requirements

• Degree in medicine, science, or a related field; a PhD is advantageous
• Relevant professional experience, ideally with minimum 2 years of clinical trial monitoring preferred
• Proficiency in both written and spoken German and English; additional fluency in French or Italian is highly desirable
• Excellent understanding of ICH-GCP guidelines and applicable regulations
• Strong understanding of diverse medical therapeutic areas, including familiarity with medical terminology
• Proven ability to communicate effectively, both verbally and in writing
• Well-developed critical thinking and analytical skills
• Exceptional organizational and problem-solving abilities
• Demonstrated capacity to deliver high-quality results within established timelines
• Ability to manage multiple projects simultaneously and prioritize effectively
• Willingness and availability to travel, both nationally and internationally

We offer

• An interesting and versatile role in a growing department, contributing to the successful development of the DCR.
• An international and dynamic environment with a motivated and diverse team, dedicated to high quality research.
• A good work-life balance thanks to flexible working hours and the possibility of working from home
• Opportunities for further training and programs within the University and a wide range of sports activities through 'Uni Sport'
• Salary and comprehensive social benefits according to cantonal guidelines.

Contact

If you have any inquiries, please contact Sophie Mermoud, a.i. Head of Monitoring Division, at Write an email.

Are you interested? Then please send us your online application to HR Administration
(Write an email) by May 8th, 2025, at the latest.