Clinical Project Manager
Job based in Shaffhausen, Switzerland
The Clinical Project Manager (CPM) makes a substantial contribution to the management of ongoing clinical trials and leads study planning, set up and execution in countries outside of the Americas. The CPM ensures the trial is conducted in compliance with the protocol, ICH/GCP and all applicable regulatory requirements.
Specific responsibilities include:
Providing oversight of site management by CROs including quality control visits and the review of monitoring visit reports. Acting as primary point of contact for vendors, investigational sites and cross functional teams.
Supporting and leading the development of clinical study plans, presentations and study-related documents including contracts. Performing in-house review of clinical data listings for completeness and accuracy. Tracking and reporting the progress of assigned projects. Contributing to the continuous improvement of departmental working practices and SOPs.
Successful candidates will have:
BA/BSc or higher degree in a scientific discipline or equivalent training and experience.
A minimum of 2 years of clinical trial experience in a pharmaceutical, biotechnology, CRO and/or healthcare setting.Prior monitoring or equivalent experience. Experience in oncology is a plus.
The ability to establish priorities and to act with a sense of urgency.
Strong communication and interpersonal skills.
Language requirement fluent English, other languages are a plus.