Clinical Data Associate II (Argentina Only - Remote) Syneos Health is a leading fully integrated biopharmaceutical... project(s). Reviews and adheres to the requirements of study-specific Clinical Data Management Plans for assigned project...
The Clinical Trial Manager II (CTM II), Dermatology & Rheumatology, is responsible for the operational management... but is not limited to clinical research associate (CRA) training, identification of quality issues related to site performance...
Study Start Up Associate II ICON plc is a world-leading healthcare intelligence and clinical research organization..., and we welcome you to join us on our mission to shape the future of clinical development. Responsibilities: - Proficient knowledge of ICON SOPs/WPs, ICH/GCP...
of clinical development. We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team.... As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting...
future of clinical development. We are currently seeking a Clinical Research Associate II to join our diverse and dynamic... team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing...
and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues... of appropriate site source documents and medical records. Verifies required clinical data entered in the case report form (CRF...
CRA I, CRA II, or Senior CRA (Single-Sponsor) ICON plc is a world-leading healthcare intelligence and clinical... shape an industry. As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment...
/patient's safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations... Document Review of appropriate site source documents and medical records. Verifies required clinical data entered in the case...
confidentiality of each subject/patient. Assesses factors that might affect subject/patient’s safety and clinical data integrity... and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies...
. Assesses factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site... required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely...
factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site... required clinical data entered in the case report form (CRF) is accurate and complete. Applies query resolution techniques remotely...
confidentiality of each subject/patient. Assesses factors that might affect subject/patient’s safety and clinical data integrity... and medical records. Verifies required clinical data entered in the case report form (CRF) is accurate and complete. Applies query...
Study Start Up Associate II ICON plc is a world-leading healthcare intelligence and clinical research organization..., and we welcome you to join us on our mission to shape the future of clinical development. Responsibilities: Proficient knowledge of ICON SOPs/WPs, ICH/GCP...
Study Start Up Associate II ICON plc is a world-leading healthcare intelligence and clinical research organization..., and we welcome you to join us on our mission to shape the future of clinical development. Responsibilities: - Proficient knowledge of ICON SOPs/WPs, ICH/GCP...
Delivery IQVIA A leading clinical research organization seeks an Associate Clinical Lead in Buenos Aires to oversee clinical... to join our Clinical Trial Management Group in Buenos Aires, Argentina. Our therapeutic areas of focus include Oncology,... Clinical...