Recibir nuevas ofertas de empleo por email
- 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....
- ...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
- ...The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference...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
- Work Schedule Standard (Mon-Fri) Environmental Conditions Office Monitors investigator sites with a risk-based monitoring approach: applies root Functions cause analysis (RCA), critical thinking and problem-solving skills to identify site processes...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...
- ...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
- ...CRA I & 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...
- ...appropriate education training and/or directly related experience will be considered sufficient for an individual to meet the requirements of the role. CRA must have adequate neurology monitoring addition rare disease and pediatric experience is strongly advised....
- ...accurate and that study materials are stored securely and per protocol requirements. Ensures adherence to global quality control and CRA performance metrics. Ensures audit readiness at site level. Acts in the project role of a Lead CRA as assigned. General On-...
- ...communication to ensure project objectives, deliverables and timelines are met. Must be able to quickly adapt, with the oversight of the Lead CRA, to changing priorities to achieve goals / targets. May act as primary liaison with project site personnel, or in collaboration...
- A leading biopharmaceutical solutions organization is seeking a CRA II for a Home-Based position in Argentina. The role focuses on site management activities including remote monitoring, ensuring compliance with regulations, and supporting patient recruitment. Ideal candidates...
- ...CRA II (Multi-sponsor) - Argentina Home Based Description CRA II (Multi-sponsor) - Argentina Home Based Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical...
- A global academic clinical research organization in Argentina is hiring a Clinical Research Associate for a remote full-time freelance role. Responsibilities include data verification, site visits, and adhering to clinical regulations. The ideal candidate has at least 2...
- ...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...Trabajo remoto
- ...revolucionando la forma de invertir en inmuebles y ahora mismo estamos en búsqueda de un perfil de Marketing Automation para que Inversor PRO, CRA, MRE y futuras líneas de negocio escalen sin fricciones, sin depender de tareas manuales, y con un funnel robusto, trazable y...
- ...The role is accountable for performance and compliance for assigned protocols and sites in Argentina. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations our company policies and procedures quality...
- ...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...
- ...other related field Typically requires 0 - 2 years of prior relevant experience on site management (Site Coordinator experience or CRA experience) - with visit coordinator skills or relevant project management experience If you are based in Argentina you need to...
- ...inbound) with sites. To monitor site performance and implement action plans for sites not meeting expectations in conjunction with the CRA. To assist CRAs with preparation for site visits (i.e. running reports QC of files (checking for missing documents) resolving...
- ...the world of today. TRIO is looking for a Clinical Research Associate to join our Monitoring Resource team. Reporting to the CRA Line Manager, this position will be a remote full-time freelance position based in Argentina . Responsibilities: Performing data...
- ...Hybrid position in Buenos Aires Only CVs in English will be considered We are looking for a CRA to join our team in Argentina. Here you will have the opportunity to develop yourself as a senior trainer mentor and leader. We are committed to develop our employees...
- ...If you are currently a CRA I looking forward to the next step of your career this might be the right position for you! As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications...
- ...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,...
- ...and/or Contract Research Organizations) with specific experience in clinical documentation and/or records & information management. CRA experience is a plus Demonstrated success in planning and executing cross functional projects. High organizational awareness...
- ...engagement activities and outcomes. Your profile Bachelor's degree in life sciences or a related field. Previous experience as CRA II or Sr CRA Based in Buenos Aires Strong interpersonal and communication skills, with the ability to build rapport and...Trabajo remoto
- ...The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), International Conference...Trabajo remoto
- ...welcome you to join us on our mission to shape the future of clinical development. 弊社の臨床開発部門において、臨床試験におけるCTM業務(主にグローバル試験)をお任せいたします。 ※CRA、他内勤ポジション等ラインマネジメント業務は、弊社のClinical Operations Managerが別途行います。 ※弊社のフルサービス部門もしくはFSP部門いずれかへの配属を想定しています。 [具体的には] 臨床試験の運営管理全般 モニタリング...
- ...point for communications with investigator site staff and may interact with principal investigators or other site staff. May accompany CRA team members to sites for observation or conflict resolution. Collaborates with functional leaders (Study Start‑Up, Patient...
- ...as well as the clinical monitoring deliverables of clinical trials. This includes but is not limited to clinical research associate (CRA) training, identification of quality issues related to site performance and clinical monitoring activities, establishing action plans...
