PSI CRO AG is a global, full-service Contract Research Organization renowned for its reliable patient enrollment and on-time project delivery across diverse therapeutic areas.
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PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense' CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com
On-site · Toronto
The Lead Clinical Research Associate coordinates site feasibility, study startup, and monitors project timelines while ensuring data integrity and compliance. They also manage project teams, oversee site monitoring visits, and act as the primary communication link between various stakeholders.
On-site · Toronto
Coordinates site feasibility, startup, and monitoring activities while managing project timelines and patient enrollment. Acts as the primary communication link between monitors, project leads, and trial sites to ensure data integrity and regulatory compliance.
On-site · Toronto
The Senior Clinical Research Associate will conduct onsite monitoring visits, perform CRF reviews, and manage site communications. They will also support regulatory document preparation and participate in study audits and inspections.
On-site · Toronto
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.