At a Glance
- Tasks: Conduct site monitoring visits and manage communication with project teams.
- Company: Dynamic global company dedicated to improving lives through medical science.
- Benefits: Competitive salary, professional development, and a supportive work environment.
- Other info: Great opportunity for skill development and career growth in clinical research.
- Why this job: Join a passionate team making a real impact in clinical research.
- Qualifications: Degree in Life Sciences and experience in monitoring visits required.
The predicted salary is between 120000 - 150000 $ per year.
- Compensation: CAD 120,000 - CAD 150,000 - yearly
- 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, COVonsite 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
- Experience in all types of monitoring visits in Phase II and/or III
- Experience in Oncology is a plus
- Full working proficiency in English.
- 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.
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Senior Clinical Research Associate in Toronto employer: PSI CRO
At PSI, we pride ourselves on being an exceptional employer, offering a collaborative work culture that fosters innovation and professional growth. As a Clinical Project Management Lead, you will benefit from our commitment to employee development, competitive compensation, and the opportunity to make a meaningful impact in clinical research across North America. Join us in a dynamic environment where your leadership will drive success and contribute to advancements in healthcare.
