Department of Clinical Research
Start date preferentially as soon as possible.
Senior Clinical Trial Monitor
Duties and responsibilities
* 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
* Provide training and lectures for various courses related to clinical research
Requirements
* Degree in a scientific field
* Relevant professional experience, ideally with a minimum of 2 years of clinical trial monitoring
* Full professional proficiency in written and spoken German and English, working knowledge of French or Italian
* Excellent understanding of ICH-GCP guidelines, ISO, and applicable regulations
* Strong understanding of diverse medical therapeutic areas, including familiarity with medical terminology
* Experience with R programming preferred
* Excellent verbal and written communication skills
* Strong critical thinking and analytical skills
* Outstanding organizational skills with a proactive, solution-oriented mindset
* Proven ability 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
* Confidence and willingness to prepare and deliver presentations
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.
Are you interested? Then please send us your complete application to HR Administration .
Required application documents:
* CV
* Motivation letter
* Academic transcript/record of grades
* Mentioning your earliest possible start date
Note: Only complete applications will be considered. jida2f18b4a jit0105a jiy26a