If you are seeking an opportunity to apply your clinical project management skills to a different research environment, we have a role that will spark your interest. Our client is a world leader in outcomes research studies and is now expanding their team as a result of continued business growth.
Our client's studies are not one size fits all and each must be designed and managed in a way that meets its specific purpose(s). Regulatory bodies are increasingly asking for long-term follow-up data on new medical products, whether it is a study of safety, benefit-risk management, outcomes and health economics, clinical and cost effectiveness, or quality.
Project Manager / Senior Project Manager
Project managers joining this team musthave managed large international studies and have a strong understanding of global project goals. With regulatory authorities increasingly calling for long-term follow-up data to justify safety, efficacy and cost-effectiveness claims, this is a secure^area of research where the need for experienced operations staff is increasing. As a Project Manager, you will coordinate and manage all deliverables, milestones and deadlines related to assigned studies/projects, including site enrolment, regulatory and IRB/EC approvals and patient enrolment and follow-up.
To be considered for these roles, candidates must have a medical or life sciences degree with at least 2 years of Project Management experience; proven management of large scale international studies; excellent communication and leadership skills; phase IV experience and EDC experience will be a distinct advantage
Fluency in English is critical and fluency in at least one other European language will be an asset.
Our client is^based in French-speaking Switzerland, near lakes and mountains, and with access to excellent international schools.