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.
We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:
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.
The Associate Director, Clinical Operations will oversee the implementation and execution of clinical trials, ensuring compliance with regulations and alignment with corporate objectives.
The Senior Specialist in Study Start Up and Regulatory Affairs leads site initiation readiness, ensuring compliance and serving as a liaison among teams and stakeholders.
The Senior Specialist in Study Start Up and Regulatory Affairs leads site initiation readiness, ensuring compliance and coordinating activities across internal teams and stakeholders.
The Senior Specialist in Study Start Up and Regulatory Affairs leads site initiation readiness, ensuring compliance and coordination among teams, clients, and stakeholders.
The Senior Specialist in Study Start Up and Regulatory Affairs leads site initiation readiness, ensuring compliance and serving as a liaison among teams, clients, and stakeholders.
