We are seeking a highly motivated team member to join our Clinical Operations team in Zurich as a Clinical Research Associate.
Main Responsibilities:
* Collaborate with study-assigned Clinical Research Manager (CRM) to ensure timely delivery of clinical investigations.
* Maintain adherence to required quality standards and laws/regulations.
* Conduct independent monitoring visits, including site qualification, study site initiation, routine monitoring, and study site closure visits.
* Verify source data and resolve queries in a timely manner.
* Assist in investigation start-up activities, such as site selection visits and review of regulatory documents.
* Maintain regular contact with investigators and the ethics committee as needed.
* Prepare and maintain investigator files, center files, and study master files.
* Communicate project-specific information to/from trial sites and document communication with investigation teams.
* Present at investigator meetings, other study trainings, and meetings as assigned.
* Support statistical evaluation of study results within clinical operations.
* Deliver clinical documentation needed for product development projects, such as clinical investigation reports.
* Screen and identify business- and product-relevant scientific literature as assigned.
Job Requirements:
* A medical-related scientific degree (e.g., Bachelor, Master, Nursing qualifications).
* Strong knowledge of ISO 14155-GCP and ICH-GCP Guidelines.
* Minimum 1-2 years of experience in various clinical trial activities within the medical device industry, preferably dentistry.
* Knowledge of the dentistry sector and strong scientific understanding are preferred.
* Excellent interpersonal skills.
* Ability to work independently and collaboratively within a team.
* Fluency in English (reading and writing); additional languages are an advantage.
* Strong interest in data analysis, graphing, and plotting results, as well as report writing.
* Willingness and ability to travel, as required (25%).
About Nobel Biocare: