Clinical Research Associate (CRA) – Oncology & General Medicine

Live Well Homecare Agency, LLC; Toronto; Vor Ort; CAD 70.000 - 100.000; Vollzeit

Zusammenfassung

Live Well Homecare Agency, LLC is seeking experienced Clinical Research Associates to lead and support a Full Service Outsourcing team overseeing oncology or ophthalmology trials across Canada. Bilingual (French-English) candidates and Sr. CRAs are highly desirable.

This role involves conducting 8-10 site visits per month across Canada, including travel support. Responsibilities include monitoring sites, ensuring protocol adherence and patient safety, regulatory compliance, SAE reporting, data

Qualifikationen

• University or college degree or relevant health professional certification.
• 1-3+ years of clinical monitoring experience, preferably in Oncology or Ophthalmology.
• Open to candidates across various Canadian hubs; French language skills preferred.

Aufgaben

• Monitoring all aspects of study sites, including routine visits, site close-outs, study file maintenance, and vendor liaison.
• Managing site activities per project plans, ensuring protocol adherence, patient safety, and data integrity.
• Verifying informed consent and regulatory compliance, reviewing source documents, and managing registry tasks.
• Handling SAE reporting, performing CRF reviews, and resolving data queries.
• Training new staff, coordinating clinical projects as a Local Project Coordinator, and supporting other duties as assigned.

Kenntnisse

Clinical monitoring

Oncology

Ophthalmology

Bilingual French-English

Regulatory compliance

Fr-English bilingual

EDC systems

Ausbildung

University or college degree

Tools

EDC systems

Jobbeschreibung

We are seeking experienced Clinical Research Associates (CRAs) to lead and support a Full Service Outsourcing team overseeing clinical trials, with a focus on Oncology or Ophthalmology. Bilingual (French-English) candidates and CAR-T experienced Sr. CRAs are highly desirable. This role involves conducting 8-10 site visits per month across Canada, including travel support.

Key responsibilities include:

• Monitoring all aspects of study sites, including routine visits, site close-outs, study file maintenance, and vendor liaison.
• Managing site activities per project plans, ensuring protocol adherence, patient safety, and data integrity.
• Verifying informed consent and regulatory compliance, reviewing source documents, and managing registry tasks.
• Handling Serious Adverse Event (SAE) reporting, performing CRF reviews, and resolving data queries.
• Training new staff, coordinating clinical projects as a Local Project Coordinator, and supporting other duties as assigned.

Qualifications include:

• University or college degree or relevant health professional certification.
• 1-3+ years of clinical monitoring experience, preferably in Oncology or Ophthalmology.
• Open to candidates across various Canadian hubs; French language skills preferred.

The role requires:

• Ability to work in a fast-paced, dynamic environment with changing priorities.
• Strong teamwork, communication, and technological skills, with proficiency in electronic data collection.
• Physical capability for extended sitting, occasional travel, and light lifting.
• Consistent attendance and adaptability to varied working hours.