Clinical Research Associate

Náplň práce, právomoci a zodpovednosti:
Key ResponsibilitiesSite & Study OperationsConduct or support site selection, initiation, monitoring, and close-out visitsEnsure compliance with protocols, ICH-GCP, and regulatory standardsMonitor patient recruitment, data collection, and site performanceMaintain accurate trial documentation and audit readinessLiaise with the internal team for study coordination and reportingSite & Investigator ManagementBuild and maintain strong working relationships with investigators and site staffProvide protocol and GCP training to site teams when requiredSupport ethics submissions and site-level regulatory processesDocumentation & ComplianceTrack site status and ensure timely resolution of queriesEnsure all documentation is inspection-ready and compliant with internal SOPsParticipate in project meetings and provide site-level updates

Zamestnanecké výhody, benefity:
Benefits:Flexible working hoursSick Days/Paid Time OffLaptop for Office useFree Drinks( coffee, Tea, Water)Health Insurance Employee TrainingAny additional benefits specified by the law.

Požiadavky na zamestnanca:
Qualifications:​​​​Bachelor’s or Master’s in Life Sciences, Pharmacy, Cosmetic Technology, or a related field2–4 years of experience in clinical research (CRA, site monitor, or similar role)Dermatology or cosmetic study experience is a strong plusKnowledge of ICH-GCP and local regulatory frameworksEnglish language proficiency: minimum B2 levelStrong organisational and communication skills​Skills Required:Strong experience in clinical trial operations, preferably in cosmetic/dermatology studies.Excellent knowledge of ICH-GCP, regulatory guidelines, and SOP-driven processes.Strong leadership, team management, and mentoring capabilities.Ability to manage multiple projects, timelines, and stakeholder expectations.Strong verbal and written communication skills.Problem-solving mindset with attention to detail and quality.