Conduct feasibility, pre-study visits, site initiation visits, monitoring visits and/or close out visits as necessary
Ensure that the monitoring team is trained on study specific procedures and aspects
Coordinate and oversee project activities
Manage the vendors involved in the study
Ensure that the monitoring activities are conducted as well as regularly reviewing the activity of monitoring, remote monitoring, contact and telephone contact reports
Update and check the Trial Master File (TMF) of the studies within Switzerland as well as ensuring that the site TMF are checked by the monitoring team according to CRO and Sponsor procedures
Degree in a scientific field
In depth knowledge of GCP and techniques for the monitoring of clinical trials
At least 5 years working as a Clinical Project Manager
Fluent in German
Able to coordinate all the activities related to the management of local and international projects including managing interventional clinical trials, monitoring of clinical trials, and guaranteeing the security of information; preferably in CRO environment
Work independently under the supervision of the Head of Clinical Operations Unit and Clinical Operations Manager
Ability to interact with personnel properly and to manage the monitoring activities of CRAs (if required)
If you are interested in discussing this role in further detail, please don’t hesitate to apply or reach out to me: Roxanna.email@example.com / +44 1273 952187.
Salary: On application
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