Clinical Site Associate, Bucharest Romania, Office based with Flex ICON plc is a world-leading healthcare..., and we welcome you to join us on our mission to shape the future of clinical development Clinical Site Associate (CSA) We are currently seeking a Clinical Site...
Clinical Research Associate ( CRA II or Senior CRA) - Remote - Romania ICON plc is a world-leading healthcare... intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence...
Clinical Research Associate ( CRAII or Senior CRA) - Remote - Romania ICON plc is a world-leading healthcare... Associate is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies...
Clinical Research Associate ( Oncology) - Hybrid - Bucharest, Romania ICON plc is a world-leading healthcare... to join our diverse and dynamic FSP team in Romania. As a Clinical Research Associate at ICON Plc, you will play a critical role...
Senior Clinical Research Associate - Sponsor Dedicated IQVIA Romania is looking for talented and motivated team..., strong career within our organization. Your responsibilities will include: Performing site selection, initiation, monitoring...
Join us in our exciting journey! IQVIA is looking for a Clinical Research Associate to provide service to the... Society for Clinical Research Sites (SCRS) for the fourth consecutive year. A site-nominated award recognizing contract...
Clinical Research Associate IQVIA Bucharest is looking for talented and motivated team member to join our Sponsor... within our organization. Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits...
Clinical Research Associate ( CRA II or Senior CRA) - Romania ICON plc is a world-leading healthcare intelligence... and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence...
Career Category Clinical Development Job Description Purpose Provide clinical site contracting services... process for clinical site contracts and clinical trial related consulting agreements (including contracts, amendments...
and motivates the site staff and principal investigator on the goals of the clinical trial program, protocol, and patient treatment... for all safety events by site personnel. Ensures audit and regulatory inspection readiness at assigned clinical site at all times...
. Strong understanding of clinical development, patient recruitment, and site engagement. In‑depth knowledge of GCP/ICH and applicable...Be the strategic force behind patient‑centric trial success at IQVIA At IQVIA, we are reimagining how clinical trials...
. Assesses factors that might affect subject/patientâs safety and clinical data integrity at an investigator/physician site... such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP...
/patientâs safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations... and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assesses site processes. Conducts Source Document...
. Assesses factors that might affect subject/patientâs safety and clinical data integrity at an investigator/physician site... such as protocol deviation/violations and pharmacovigilance issues. Per the Clinical Monitoring/Site Management Plan (CMP/SMP...