ICON plc Jobs in Canada

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advance ...

+This is a full-time hybrid role for a Clinical Research Associate based in Toronto, ON. · +Oversight of clinical trials · Maintenance of regulatory compliance · Collections and verification of trial data · ...

Senior Clinical Research Associate, Bilingual, QuebecICON 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 ...

We are seeking a Project Manager to join our diverse and dynamic team. As a Project Manager at ICON, you will be responsible for leading and coordinating project activities, ensuring that projects are delivered on time, · within budget, and to the highest quality standards. · We ...

Se busca un Clinical Research Associate con experiencia en la industria farmacéutica o CRO para trabajar en Toronto. · Servir como punto de contacto principal entre los sitios de estudio y el patrocinador. · Conducir todas las tipos de visitas a sitios, incluyendo selección, inic ...

Contribute to the development of study documents as appropriate. Lead the preparation of country specific agreements, confidentiality agreements, clinical trial applications and other applicable country documents. · Manage third-party vendors assessing initial statement of work a ...

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. Responsible for the successful negotiation and on-going maintenance of clinical trial agreements. · ...

+Clinical Research Associate (CRA) role at ICON plc involves conducting site visits including evaluation initiation monitoring close out overseeing reporting conduct of clinical trials at site level maintaining solid professional relationships with site staff facilitating subject ...

We're seeking a Lead Clinical Data Science Programmer to join our diverse and dynamic team. As a Lead Clinical Data Science Programmer at ICON, you will play a key role in designing and developing clinical data solutions, ensuring the efficient handling, analysis, and reporting o ...

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. · The Study Manager will assist with the operational conduct of clinical studies. · Assists the SM Study L ...

We're proud to foster an inclusive environment driving innovation and excellence. · We welcome you to join us on our mission to shape the future of clinical development.University degree (or equivalent), preferably in medical or biological sciences or discipline associated with c ...

The Grants Manager is responsible for the overall management of the grants and sponsorships program in Global Medical Affairs. · This role will have responsibility for queries around the submission and review process, including cross-functional training to key internal stakeholde ...

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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. · Our success depends on the quality of our people. That's why we've made it a priority to build a diverse c ...

Clinical trial associate to support the design, implementation and management of clinical trials. · ...

Clinical Research Lead (Site Engagement) 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 seeking a Senior Statistical Programmer II/Clinical Data Science Programmer to join our diverse and dynamic team. · Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related field. · Significant experience in statistical programming within th ...

Servez en tant qu'Associé(e) de recherche clinique dans la région occidentale du Canada. · Bachelor's degree in a scientific or healthcare-related field. · Minimum of 2 years of experience as a Clinical Research Associate. · ...

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing ...

We are currently seeking a Clinical Research Associate with at least two years of on-site monitoring experience to join our diverse and dynamic team.Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) s ...