EPM Scientific are currently working with a leading, cutting edge Global CRO with an exciting specialized pipeline seeking a Consultant Clinical Research Associate (contractor) to join their team.
Quick facts:
Start date: ASAP
Location: Switzerland
Interviews: As soon as possible
Language: English, German is a plus
Project: Medical Device
Key Responsibilities:
Perform site qualification, initiation, monitoring, and close out visits
Ensure compliance with study protocols, regulatory requirements
Maintain accurate and organized documentation of all site visit activities
Collaborate with investigators, site staff, and sponsors to ensure smooth trial execution
Assist in the preparation and submission of regulatory documents
Required Experience:
Previous experience as a CRA essential
Medical Device experience is ideal
Strong Knowledge of good Clinical Practice (GCP)
If this role is of interest to you, please apply directly. If not feel free to share with your network.
