Founded By Science, Driven By Quality, Led By Experts
Mississauga, Ontario
Pharma Medica Research is a full service early phase contract research organization. We offer an innovative approach to the design and implementation of clinical trials in support of pharmaceutical and biotechnology companies' drug development projects around the globe. * 360 bed phase I clinical capacity * Bioanalytical lab * Onsite organic synthesis lab * Biorepository services * Clinical data management * Medical writing * PK / Biostatistics * Clinical trial monitoring In addition to FIH, BA/BE, and PK/DDI studies, we have specialized skills in respiratory, transdermal delivery systems (including SIS studies), and patient PK studies. Our reputation is built upon principles of on-time performance, responsiveness to the industry we serve, and delivery of uncompromising quality at reasonable costs. Our client-focused approach truly differentiates us from other contract research organizations. Pharma Medica Research has developed processes that put the needs of our clients first. These include flexible study scheduling, rapid preliminary results turnaround and prompt final report delivery. Outsourcing should not be complicated. We are there to make your project implementation as simple as possible.
Hybrid · Toronto
Lead recruitment operations for Phase I clinical trials by managing on-site and remote call center staff to ensure timely participant enrollment. Monitor performance metrics, optimize marketing strategies, and maintain accurate participant databases to meet study goals.
On-site · Mississauga
The Project Manager is responsible for managing clinical trial progress, preparing study quotations and contracts, and maintaining client communications. They coordinate activities across various PMRI divisions to ensure timely delivery of project milestones and adherence to contractual deadlines.
On-site · Mississauga
The IT Helpdesk Administrator will serve as the primary point of contact for IT support, managing hardware, software, and network access for users. They are also responsible for maintaining IT asset inventory, documenting standard operating procedures, and administering Microsoft 365 and Intune environments.
On-site · Scarborough
The Medical Recruiter is responsible for telephone screening potential study participants and managing participant files within the PSMS system. They will also handle participant inquiries, book appointments, and ensure all clinical documentation complies with GCP and SOP guidelines.
On-site · Scarborough
Perform clinical procedures including blood sample collection, processing, and storage according to study protocols and SOPs. Monitor subject safety and maintain clinical documentation in compliance with GCP and regulatory requirements.
On-site · Scarborough
The Facility Assistant is responsible for maintaining the cleanliness and order of the clinic facility, including study rooms, washrooms, and administrative offices. Duties include general building maintenance, repairs, painting, and seasonal snow removal.
On-site · Toronto
Plan and supervise the execution of early phase clinical trials while performing technical functions like phlebotomy and ECGs. Ensure all study activities comply with protocols, SOPs, and GCP requirements while monitoring subject safety and adverse events.
On-site · Mississauga
The Lab Support Services Assistant is responsible for managing study samples, including receipt, storage, and disposal, while ensuring compliance with GLP and SOP requirements. They also maintain laboratory inventory, monitor equipment temperatures, and provide general support to the Bioanalytical lab operations.
