Beschreibung:

Job Responsibilities Monitoring independently different sites, including RBM.Participation in investigator meeting as necessaryEnsuring the trial is conducted in accordance with the approved protocol ICH-GCP guidelines, SOPs etcEnsuring effective communication between investigational sites and internal/external stakeholdersWorking on project work and initiatives for process improvement as required Skills and RequirementsDegree in pharmacy, life science or related fieldExperience in a pharmaceutical, biotech or CRO companyIndependent clinical monitoring experienceFluency in English, German and French ideally (English and 1 of the two other languages will be accepted)Demonstrated understanding of medical/therapeutic area knowledge and medical terminologyExcellent understanding and demonstrated application of GCPs and applicable SOPsManagement of regulatory and / or IEC questionsDevelopment and preparation of the local informed consent formEffective oral and written communication skills, with the ability to communicate effectively with medical personnelProven flexibility and adaptabilityAbility to work in a team or independently as required