Senior CRA/Clinical Site Manager
3 semanas atrás
Clinical Site Manager 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. As a Senior CRA / Clinical Site Manager you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. You’ll utilize your extensive therapeutic knowledge in Oncology to oversee uniquely-focused clinical studies. Working at the core of clinical research, you’ll be exposed to cutting-edge protocols and experience a dedicated partnership with your team like never before. What you will be doing: You will monitor multiple Phase I, II, III & IV clinical trial sites You will utilize your customer service mindset with your sites focusing on delivering value, building loyalty and trust to create a positive impact and strong relationship with investigators and study coordinators where respect, knowledge and commitment to ICH/GCP guidelines are key to successful trial conduct. As the CRA you are the main sponsor representative, providing key project updates. You will collaborate with the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely. You will be first to review "source to CRF/eCRF," ensuring patient safety and data integrity aspect of the study. As the first point of contact for study sites, escalating any concerns/issues to other departments including Safety, Investigational Medicinal Product, Local Study Managers and management team as appropriate. Additionally, you will oversee the sites' adherence to GCP/ICH practices, ensuring quality of study conduct. You are: Bachelor’s Degree (or equivalent) with +4 years of relevant healthcare experience in the pharma or clinical research industry. Minimum 3/4 years of monitoring and site management experience TA: Oncology Scientific background Proficiency with medical terminology Working knowledge of Local Regulations A demonstrated working knowledge of ICH/GCP Guidelines Excellent record-keeping skills and attention to detail Experience conducting Site Selection, Initiation, Routine Monitoring and Close Out Visits both remotely and on-site Fluent in English, both written and oral and local language Strong technical skills with CTMS, eCRF, eTMF What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply #J-18808-Ljbffr
-
Clinical Site Manager Ii
2 semanas atrás
São Paulo, Brasil ICON Plc Tempo inteiroSr. CRAICON 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 developmentWe are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and...
-
Clinical Project Manager **Level Dependent on Experience**
3 semanas atrás
São Paulo, Brasil CTI Clinical Trial and Consulting Services Tempo inteiroClinical Project Manager – Level Dependent on Experience CTI Clinical Trial and Consulting Services is a global, privately held, full‑service clinical contract research organization focused on advancing treatments for chronically and critically ill patients. We support clinical research throughout the life cycle of development, from drug concept to...
-
Senior Cra
Há 14 horas
São Paulo, Brasil Icon Tempo inteiroSenior Clinical Research Associate - Remote - Brazil 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.We are currently seeking a Senior Clinical...
-
Clinical Project Manager
2 semanas atrás
Sao Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro**Clinical Project Manager****(Level Depends on Experience)****Job Purpose/Summary**: Responsible for management and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client’s goals of time, budget and quality performance are met. The Clinical Project Manager I is expected to require support and guidance from Directors and/or...
-
CRA II/Senior CRA
3 semanas atrás
São Paulo, Brasil ICON Tempo inteiroCRA II/Senior CRA, home based, Czech Republic 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. We are currently seeking a Senior Clinical Research...
-
Senior CRA
3 semanas atrás
São Paulo, Brasil ICON Tempo inteiroSenior CRA 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. We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse...
-
Senior Cra
2 semanas atrás
São Paulo, Brasil ICON Plc Tempo inteiroSenior CRA - Remote - Brazil 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 At ICON, it’s our people that set us apart. Our diverse teams...
-
São Paulo, Brasil CTI Clinical Trial and Consulting Services Tempo inteiroCTI Clinical Trial and Consulting Services is a global, privately held, full‑service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered...
-
In-house Cra I
Há 5 dias
São Paulo, Brasil Fortrea Tempo inteiro**Job Overview**:**Summary of Responsibilities**:- To serve as contact for project team and investigative sites, conduct site contacts and document contacts for assigned sites as required per study guidelines, including creating contact reports for each telephone session (outbound or inbound) with sites.- To monitor site performance and implement action...
-
Associate Director Clinical Monitoring
Há 14 horas
São Paulo, São Paulo, Brasil CTI Clinical Trial and Consulting Services Tempo inteiroAbout CTICTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is...