Clinical Trial Assistant - Montreal

L'assistant aux essais cliniques fournit un soutien à l'équipe des opérations cliniques dans l'exécution de tous les aspects des activités d'essais cliniques et d'opérations réglementaires conformément aux ICH/BPC, aux réglementations applicables et aux SOP/politiques de 35Pharma ...

We are seeking a Clinical trial Assistant for our client who is based in Laval, Quebec. In this role, you will assist the research team in planning and executing clinical studies. · Provide the necessary support for clinical trial management while complying with regulatory requir ...

+We are seeking a Clinical trial Assistant for our client who is based in Laval, Quebec. In this role, you will assist the research team in planning,, executing,, and managing clinical studies. · +Provide necessary support for clinical trial management while complying with regula ...

L'assistant aux essais cliniques fournit un soutien administratif aux gestionnaires de projet et travaille en étroite collaboration avec les sites cliniques et les installations d'IRM. · ...

This is a full-time on-site role based in Montreal, QC, · a Clinical Trial Associate will support the planning, · coordination and execution of clinical trials ensuring · that regulatory compliance and operational standards are met.Maintaining and updating the Trial Master File ( ...

We are looking for a Clinical Investigator (MD) to oversee and delegate tasks related to clinical trials under their leadership. · ...

We are seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requireme ...

The Customer Service Representative will provide volunteers with preliminary clinical trial information and company details as well as pre-screen volunteers to determine eligibility for clinical trial screening. · Ensure the confidentiality of clinical trial participants and spon ...

+ Full time position (37,5 hours/week) · + On site position at our Montreal site (1200 Beaumont) · + Altasciences is an equal opportunity employer committed to diversity and inclusion.Job summaryThe Specialized Nurse Practitioner is responsible for supervising clinical activities ...

L'Associé(e) principal(e) de recherche clinique participe à la préparation et à l'exécution des essais cliniques de phase I à IV. Il/elle supervise l'avancement des investigations cliniques en effectuant des visites d'évaluation intermédiaire, initiale et finale. · ...

Advise clients on legal proceedings and prepare wills, real estate transactions and other legal documents. · ...

Assemble documentary evidence in preparation for trial. Advise clients on legal proceedings. · Maintain filing systems · ...

We are looking for an IRT Specialist in Clinical Supply Chain. · Your mission will be to set up and maintain IRT systems, ensure quality and processes, and support study teams as overall SME for IRT tool. · You will independently configure and manage/maintain complex IRT study de ...

We are looking for talented and enthusiastic people to join our growing team at Altasciences. · ...

· Advise clients on legal proceedings Assemble documentary evidence in preparation for trial Co-ordinate administrative services Perform clerical duties such as maintain filing systems Write trial briefs Prepare wills real estate transactions and other legal documents court repo ...

Clinical Research Lead (Site Engagement) at ICON plc: Foster an inclusive environment driving innovation and excellence. · ...

We're proud to foster an inclusive environment driving innovation and excellence, · Clinical Investigator Management · Clinical Trial Management · Business Management and Engagement ...

The McGill University Gerald Bronfman Department of Oncology invites applications for a full-time position as a member of the Contract Academic Staff as a clinician teacher/clinician-investigator at the rank of Assistant or Associate Professor (Clinical) based at the Jewish Gener ...

We are seeking a Global Study Manager to join our team at ICON plc. · As Global Study Manager, you will be responsible for contributing to the development of study documents and leading the preparation of country-specific agreements and clinical trial applications. You will also ...

The Clinical Research Nurse will oversee the safety and consent of clinical trial participants during study conduct and the maintenance of safety equipment. · Perform scheduled inspection of emergency crash carts, inventory/inspect the contents, and maintain up to date records. · ...