Clinical Trial Coordinator

About the RoleWe are seeking a skilled Clinical Research Coordinator to join our team at the Rotman Research Institute. In this role, you will be responsible for coordinating and supervising all study activities, ensuring proper execution of assigned clinical research trials, and meeting regulatory requirements.The ideal candidate will have a strong...

Job SummaryWe are seeking a detail-oriented and organized Clinical Research Coordinator II to join our team. In this role, you will be responsible for coordinating and managing multiple clinical trials simultaneously, ensuring timely and accurate completion of tasks and responsibilities.Main ResponsibilitiesClinical Trial Coordination: Oversee the daily...

Role OverviewThe GCP Compliance Manager, Program is a key role within the organization responsible for ensuring the compliance of regulated activities across clinical trials. This position requires a strong understanding of regulatory requirements, excellent organizational and analytical skills, and a proven track record of delivering high-quality results in...

About UsPharma Medica Research Inc. is a leading provider of clinical trial services. Our team of experts conducts early phase clinical trials in healthy volunteers and special patient populations.We're seeking a highly skilled Medical Recruiter to join our team.

Clinical Trial AssociateThe Clinical Trial Associate will be responsible for setting up, tracking and maintaining Clinical Site related documents. You will help manage and review regulatory documents as well as maintain the Local Study File. Assist with coordinating the distribution, retrieval and review of regulatory documents required for the initiation of...

**Job Description**We are looking for an experienced Clinical Trials Statistician to support our research initiatives at Alimentiv. In this role, you will apply biostatistical methods to drive clinical trial success.**Responsibilities**Carry out statistical analyses and provide direction to programmers using standard software packages.Prepare statistical...

About the PositionThis position offers the opportunity to work on high-profile clinical trials and develop expertise in clinical development. The Senior Clinical Research Director will lead cross-functional teams to achieve clinical trial goals and objectives.Key ResponsibilitiesDevelop and implement clinical development strategies for assigned program...

Healthcare Businesswomen's Association is seeking a highly skilled Clinical Operations Coordinator to join our team. As a key member of the GCO team, you will contribute to all compliance activities supporting the three pillars of GCP Compliance, issue management, audits & inspections.About the TeamYou will work closely with Clinical Trial Teams and...

Job OverviewPharma Medica Research Inc. is a full-service contract research organization specializing in conducting early-phase clinical trials in healthy volunteers, special, and patient populations. Our team is dedicated to delivering high-quality research services and seeking talented individuals to join our growing organization.

At Ecrscorp, we are seeking a highly skilled Senior Medical Writer to join our team in Toronto/Markham, Ontario, Canada. As a Senior Medical Writer, you will be responsible for creating high-quality clinical documents, including clinical study protocols, CSRs, DSURs, integrated efficacy or safety summaries, patient narratives, manuscripts, posters, and...

Job DescriptionThis Clinical Trial Governance Lead role is responsible for driving the adoption of Risk-based Quality Management (RBQM) practice at trial level, overseeing implementation, and continuous improvement.Main Accountabilities:Risk Assessment and Mitigation: Facilitate trial protocol risk assessment across multiple cross-functional domains...

Job OverviewWe are looking for a highly skilled Risk Management Lead for Clinical Trials to join our team. As a key member of our organization, you will be responsible for driving the adoption of Risk-based Quality Management (RBQM) practices at trial level, overseeing implementation, and ensuring continuous improvement.The ideal candidate will have a strong...

About Us\Pharma Medica Research Inc. is a leading contract research organization specializing in early phase clinical trials for healthy volunteers, special populations, and patients.\We are currently seeking an experienced Clinical Research Coordinator to join our team at our clinic location in Scarborough.\Job Description\The Study Coordinator will...

Required Skills and QualificationsTo succeed in this challenging role, you will need to possess a strong background in clinical research, with at least 10 years of experience in global drug development spanning phases I through IV. Your expertise should encompass all aspects of conducting clinical trials, including planning, execution, reporting, and...

About the RoleWe are seeking a highly motivated and detail-oriented Clinical Research Coordinator I to join our team. In this role, you will work closely with the Principal Investigator and study team to coordinate various aspects of human subject research, including regulatory activities, data management, and participant recruitment.Main...

Job RequirementsWe are seeking a highly motivated and detail-oriented Study Coordinator to join our team at Pharma Medica Research Inc.About the PositionThis role is responsible for supervising the planning and conduct of clinical studies, ensuring compliance with protocols, SOPs, and GCP. The ideal candidate will have excellent organizational skills, be...

Job OverviewPharma Medica Research Inc. is a full-service contract research organization specializing in early phase clinical trials. We are seeking an experienced Study Coordinator to join our team in Scarborough.About the CompanyAs a contract research organization, we provide comprehensive services to pharmaceutical and biotechnology companies. Our mission...

Key Job ResponsibilitiesThe Trial Quality Assurance Manager will be responsible for driving the adoption of Risk-based Quality Management (RBQM) practices at trial level, overseeing implementation, and ensuring continuous improvement. This includes facilitating trial protocol risk assessments, defining quality tolerance limits, and ensuring mitigation...

Overview\ \Ecrscorp, a leading contract research organization (CRO), is seeking an experienced Clinical Trial Web Application Developer to join our team in Toronto/Markham, Ontario, Canada or remotely from a home-based office anywhere in Canada. As a key member of our clinical research team, you will be responsible for designing, developing, and maintaining...

Job Description SummaryThe Senior/Clinical Development Director (Sr. CDD) is the clinical/scientific expert and, if assigned, the clinical development lead of a section of a global clinical program and/or trial (e.g., an indication, a new formulation, or a specific development phase) or a large, complex trial, under the leadership of the GPCH. The Sr. CDD...