Empleos de Cra

 ...innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements... 

JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Research Associate I – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical...

CRA II Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate... 

 ...CRA I ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.... 

 ...CRA II - Argentina ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical... 

 ...The Senior Clinical Research Associate (CRA) will play a crucial role in the planning, execution, and management of clinical trials. This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data, compliance with regulatory... 

 ...assure that the site is in compliance with the protocol and is inspection ready. The Senior Clinical Research Associate I (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient... 

 ...driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a CRA I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across... 

 ...Whether you're beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You'll have training and development to plan and progress your career in the direction you choose. And you won't do it alone - you will have dedicated mentoring and receive... 

 ...are aligned to the critical path for site activation. • Achieves PPD’s target cycle times for site. • May work with the start-up CRA(s) to prepare the regulatory compliance review packages, as applicable. • May develop country specific Patient Information Sheet/Informed... 

 ...the study commitments within the country and for timely delivery of data to required quality. Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies. Leads and optimizes the performance of the Local Study Team(s) at country level ensuring... 

 ...and or audits of the Trial Master File (TMF) to ensure inspection readiness. May support clinical monitoring activities, such as CRA training, visit report review, site letters, and escalated site issues May track site qualification, initiation, routine and close... 

 ...Pharmacy, Biotechnology, QFB (Chemical Pharmaceutical Biology) or related health sciences Minimum 2 years of proven experience as a CRA monitoring clinical trials Intermediate to advanced English proficiency (written and spoken) Solid working knowledge of ICH-GCP... 

 ...language of study sites, facilitate site negotiations and communications through the use of an intermediary party (i.e., sub-CRO or CRA) Provide oversight to Sub-CROs on contracting activities, as required Make all efforts to ensure total study budget is respected... 

 ...Clinical Research Associates and Senior Clinical Research Associates to join our growing team. The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s).... 

 ...forecasting. Contribute to study meetings, Investigator Meetings, feasibility assessments, and, when required, local project management, CRA support, and bid defense activities. Qualifications:  ~ Minimum 5 years of clinical monitoring experience in a CRO,...