Senior Clinical Research Associate

Job summary

The Senior CRA is responsible for conducting onsite monitoring visits, including SIV, RMV, and COV, while managing site communications and CRF reviews. They also support regulatory submissions, participate in feasibility research, and prepare for audits and inspections.

Job details

Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada: Conduct and report SIV, RMV, COV onsite monitoring visits Perform CRF review, source document verification and query resolution Be responsible for site communication and management Be a point of contact for in-house support services and vendors Communicate with internal project teams regarding study progress Participate in feasibility research Support regulatory team in preparing documents for study submissions Prepare and particiapte on audits and inspections Qualifications College/University degree in Life Sciences or an equivalent combination of education, training & experience Independent on-site monitoring experience Experience in all types of monitoring visits in Phase II and/or III Experience in Oncology is a plus Full working proficiency in English and French. Proficiency in MS Office applications Ability to plan, multitask and work in a dynamic team environment Communication, collaboration, and problem-solving skills Ability to travel Valid driver’s license Additional Information For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future. This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research. Compensation: CAD 120000 - CAD 150000 - yearly

What you’ll do

The Senior CRA is responsible for conducting onsite monitoring visits, including SIV, RMV, and COV, while managing site communications and CRF reviews. They also support regulatory submissions, participate in feasibility research, and prepare for audits and inspections.

Requirements

Candidates must hold a degree in Life Sciences and have independent on-site monitoring experience in Phase II and/or III trials. Full working proficiency in both English and French, along with a valid driver's license, is essential.

Listed skills

• Problem solving · Preferred
• Collaboration · Preferred
• MS-Office · Preferred
• Multitasking · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• On-site Monitoring
• CRF Review
• Source Document Verification
• Site Management
• Feasibility Research
• Regulatory Documentation
• Audit Preparation
• Oncology
• English Proficiency
• French Proficiency
• MS Office
• Multitasking
• Problem-solving
• Collaboration
• Clinical Research
• Project Communication

Job areas

• Healthcare
• Science & Research