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.
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 · Mississauga
Responsible for writing safety and efficacy conclusions in Clinical Study Reports (CSR) and contributing to regulatory documents for Phase I-III studies. The role involves reviewing clinical documentation, collaborating with cross-functional teams to generate protocols, and ensuring compliance with regulatory guidelines.
On-site · Toronto
The Director plans and oversees various clinical department activities including facility management, clinic assistants, administration, and supply maintenance. They are responsible for supervising managers, ensuring regulatory compliance, and maintaining high standards for clinic service provision.
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 · Mississauga
The Assistant Project Manager is responsible for keeping clients informed of clinical trial progress and preparing study quotations and contracts. Additional responsibilities include assisting with regulatory document preparation and tracking the progress of ongoing studies.
On-site · Mississauga
The Senior Pharmacokinetic Scientist performs pharmacokinetic and pharmacodynamic analyses of clinical study data and mentors junior staff. They also assist in study design, review protocols, and ensure compliance with regulatory guidelines.
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.
