Company Description PSI is a leading Contract Research Organization with more 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time
Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow
Company Description Traferox creates, manufactures and commercializes products for organ transplantation (lungs, heart, liver, kidneys, pancreas). These products employ technologies invented by transplant surgeons at partnering institutions, translating impactful clinical innovations into new standards of care.
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 company founded in 1995, we bring
Summary The Clinical Research Associate will perform monitoring and site management activities for Phase I-IV clinical research projects to assess the progress of clinical projects at assigned investigative/physician sites (either on site or remotely) and to ensure
Base pay range CA$52,500.00/yr - CA$87,500.00/yr Responsible for the management of the Trial Master File (TMF) content and associated processes during the study life cycle from study setup to transfer/archiving. Work in partnership with study teams during
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Description The project manager II has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The project manager II oversees and coordinates study resources to ensure compliance with
Description The Project Manager II, EPTR has the overall responsibility for the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical trials. The Project Manager II, EPTR oversees and coordinates study resources to ensure
Clinical Research Associate (Study Start Up) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and
A leading clinical research organization in Canada is seeking a TMF Coordinator to manage Trial Master File processes throughout the study lifecycle. The ideal candidate will have a college diploma and 1-3 years of relevant experience, emphasizing
Senior Clinical Research Associate - Oncology - Alberta, Canada ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values‑driven organisation, integrity,
Position Summary Manage the full operational execution of clinical trials for Puzzle Medical Class III medical devices, with primary responsibility for site management, monitoring, and inspection readiness. Responsible for end-to-end delivery of Early Feasibility Studies (EFS),
Engage with our proactive talent pool for Clinical Research Associates supporting our Clinical Monitoring team. This is an invitation for individuals at varying seniority levels seeking career advancement in clinical research. As a Clinical Research Associate, you will
Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management and close‑out visits (performed on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall
Role Summary The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA
Clinical Research Associate – Canada Syneos Health® is a fully integrated biopharmaceutical solutions organization committed to accelerating clinical research and improving patient outcomes. Responsibilities Perform site qualification, initiation, interim monitoring, site management, and close‑out visits (on‑site or
Compensation: CAD - CAD - yearly Company Description PSI is a leading Contract Research Organization with more 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We
Vue d’ensemble du poste Effectuer des tâches de suivi et de gestion de site pour une variété de protocoles, de sites et de domaines thérapeutiques. Doit être bilingue français et anglais et situé à Montréal. Responsabilités
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