Senior Clinical Research Lead - Global Site Monitoring

PSI CRO; Canada; Remote; CAD 80,000 - 100,000; Full time

Job summary

A leading Contract Research Organization in Canada seeks a dedicated Lead Monitor to coordinate clinical study processes and ensure compliance in monitoring. The ideal candidate will have a relevant degree, at least 4 years of site monitoring experience in clinical projects, and strong expertise in oncology and CAR-T therapy. Excellent communication and problem-solving skills are essential. The position requires up to 65% travel.

Qualifications

• Relevant educational background in Life Sciences or an equivalent combination of education, training and experience.
• Minimum of 4 years of site monitoring experience with participation in global clinical projects.
• Must have experience monitoring or managing sites and CRAs in the United States.

Responsibilities

• Coordinates investigator/site feasibility and identification process.
• Monitors project timelines and patient enrollment.
• Reviews monitoring visit reports for compliance.

Skills

Site monitoring experience

Communication skills

Collaboration skills

Problem-solving skills

Multitasking ability

Education

MD, MPharm, RN or equivalent

Tools

MS Office

Job description

A leading Contract Research Organization in Canada seeks a dedicated Lead Monitor to coordinate clinical study processes and ensure compliance in monitoring. The ideal candidate will have a relevant degree, at least 4 years of site monitoring experience in clinical projects, and strong expertise in oncology and CAR-T therapy. Excellent communication and problem-solving skills are essential. The position requires up to 65% travel.