. trip report review, newsletter creation, lead CRA team calls etc). Provides trial status tracking and progress update...
clinical studies. As a PPD CRA, you will perform and coordinate all aspects of the clinical monitoring and site management... as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc). - Facilitates effective communication...
Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into...
Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into...
**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to lif...
OverviewSr CRA I - Sponsor dedicated - Chile Home Based role at Syneos Health.ResponsibilitiesConduct on-site... development and input on study design and methodology.Manage and direct the work of lower-level professionals or oversee day...
OverviewTitle: CRA I - Sponsor dedicated - Chile Home BasedLocation: CHL-RemoteUpdated: YesterdayJob ID... and action items.For assigned activities, understands project scope, budgets, and timelines; manages site-level activities...
have contact with investigators for submission related activities - Key-contact at country level for either Ethical or Regulatory... - May work with the start-up CRA(s) to prepare the regulatory compliance review packages, as applicable - May develop...
, data quality and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted... performing regular reviews of site level data in clinical systems (e.g. CTMS, EDC, IVRS, and SIS) and ensure timely and high...
quality and ensuring compliance with ICH GCP and local requirements at the site level. Monitoring will be conducted in line... performing regular reviews of site level data in clinical systems (e.g. CTMS, EDC, IVRS, and SIS) and ensure timely and high...
driver’s license Advanced level of English. Based in Buenos Aires. What ICON can offer you: Our success depends...Sr CRA ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster...
Updated: Yesterday Location: Buenos Aires, B, Argentina Job ID: 25102449 Description CRA II - Sponsor dedicated... activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure project...
Job Summary : Join Medpace in Buenos Aires! The Clinical Research Associate at Medpace is offering the unique... – MEDPACE CRA TRAINING PROGRAM No clinical experience is needed as Medpace provides comprehensive initial and ongoing training...
Job Summary Join Medpace in Buenos Aires! The Clinical Research Associate at Medpace is offering the unique... – MEDPACE CRA TRAINING PROGRAM No clinical experience is needed as Medpace provides comprehensive initial and ongoing training...
Updated: Yesterday Location: Buenos Aires, B, Argentina Job ID: 25102450 Description CTM I Syneos HealthÂ.... For assigned activities, understands project scope, budgets, and timelines; manages site-level activities / communication to ensure...
Updated: Yesterday Location: Buenos Aires, B, Argentina Job ID: 25102453 Description CTM II Syneos HealthÂ... or other site staff members. This may include accompanying CRA team members to sites for observation or conflict resolution...