Clinical Research Associate with experience - Sponsor dedicated - Serbia
Core
Conduct site monitoring and management to ensure clinical studies adhere to protocols, regulations, and sponsor requirements.
Role type
Clinical Research Associate (CRA)
Builds
Clinical trial data and site compliance
Domain
Life sciences / Clinical research (via careerplan.io/jobs/R1558179-clinical-research-associate-with-experience-sponsor-dedicated-serbia-at-iqvia)
Required skills
Site monitoring, subject recruitment tracking, protocol administration, regulatory compliance, TMF/ISF management, data query resolution, financial management, documentation, stakeholder liaison
Preferred skills
Bachelor's degree in scientific discipline or healthcare
Technologies
Trial Master File (TMF), Investigator's Site File (ISF), Case Report Forms (CRF)
Responsibilities
Perform site monitoring visits (selection, initiation, monitoring, close-out); Drive subject recruitment plans; Administer protocol training to sites; Evaluate site quality and adherence to GCP/ICH; Track regulatory submissions, enrollment, and data submissions; Maintain site documentation and visit reports; Collaborate with study team members; Manage site financials and invoices if applicable
Seniority
Entry-level to Junior