Clinical Research Associate (m/f)

For our customer, a leader in post-approval clinical research and quality measurement, who creates patient registries that focus on safety, effectiveness, value and quality of healthcare products, therapies and services, we are looking for a Clinical Research Associate (m/f) permanent employment in Westschweiz Reference number:

80044/11

Your Duties: Responsible to coordinate all aspects involved in investigator/site selection Collate regulatory documents, initiate, monitor and close-out of sites on assigned Phase IV/Post-Market Studies, in accordance with Sponsor requirements while working collaboratively with internal and external project teams Take the lead on smaller projects with an opportunity to advance your career as a Project Manager Your Qualifications: A Bachelor’s degree in Life Sciences or equivalent nursing qualification/experience with a minimum of 2 years clinical trial experience, including a working knowledge of Phase IV/Post Market Studies in Europe Excellent communication skills Proven decision making, problem solving and demonstrated abilities to manage multiple priorities Fluent in English, other European languages are desirable