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- CRA I 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....Trabajo remoto
- CRA II 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 (Multisponsor) 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...Trabajo remoto
- ...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...
- ...years. As part of our global team, you’ll have the opportunity to perform remote activities on assigned projects in liaison with the CRA and study Clinical Lead. As an Assistant Clinical Research Associate, you'll provide support with site preparedness, logistical...Trabajo remoto
- ...As a Study Start-Up CRA (SSU CRA) will be responsible of creating and endorsing submission packages related to the country or site, following ICH, GCP, and all relevant regulations, laws, guidelines, and ethical standards, within specific deadlines and quality standards...Trabajo remoto
- ...suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc). • Facilitates effective communication between investigative sites, the client company and the PPD project team...Trabajo remoto
- CRA II or Sr CRA Sponsor Dedicated (Argentina - Home-based) 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...
- ...puesto: Es responsable por la entrega de los estudios en los sitios asignados y participa en los equipos de estudio locales. El CRA trabaja en estrecha colaboración con otros CRA y el Equipo de estudio local / Gerente de estudio local para garantizar que los compromisos...
- ...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...
- ...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...
- ...Only CVs in English will be accepted. You will be responsible for: Being the main point of contact between site personnel and CRA involved in the project helping on query resolution and EDC completion. Serves as the primary sites’ contact point for vendors, study...
- ...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...
- ...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,...
- ...required to interact on the phone or in person with principal investigators or other site staff members. This may include accompanying CRA team members to sites for observation or conflict resolution. Collaborates with other functional leaders such as Study Start Up,...
- ...education and experience. •Preferred experience in a CRO/pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience. • Thorough knowledge of applicable regulations, drug...