National Training Coordinator, Clinical Trials

2 weeks ago


Montréal, Canada Centre universitaire de santé McGill Full time

Organization description
Le Centre universitaire de santé McGill (CUSM) est un centre hospitalier universitaire intégré, reconnu à l’échelle internationale pour l’excellence de ses programmes cliniques, de sa recherche et de son enseignement. Le CUSM a pour objectif d’assurer aux patients des soins fondés sur les connaissances les plus avancées dans le domaine de la santé et de contribuer au progrès des connaissances.
**Job Description**:
RESEARCH INSTITUTE OF THE MUHC
The Research Institute of the McGill University Health Centre (RI-MUHC) is a world-renowned biomedical and hospital research centre. Located in Montreal, Quebec, the Institute is the research arm of the McGill University Health Centre (MUHC) affiliated with the Faculty of Medicine at McGill University. The RI-MUHC is supported in part by the Fonds de recherche du Québec - Santé (FRQS).

Position summary
National Training Coordinator, Clinical trials & Regulatory affairs (C&RA) Training Programs for Postgraduate students will oversee day-to-day operations, planning, implementation, and evaluation of postgraduate student training in clinical trials & regulatory affairs. This includes coordinating the existing program’s activities, adapting the program for expansion to new centres, maintaining the program materials and e-learning assets, and communications and developing marketing strategies to maximize outreach to students.

This position reports directly to the National Director, Streams of Clinical Trials’ Training Programs and to the Associate Director of the Desjardins Centre for Advanced Training.

General Duties
1. Plans, coordinates and implements day-to-day delivery of the training program.
2. Plan and coordinate components of curricular and/or co-curricular programs and activities for graduate students and postdocs as part of the program. This includes working with clinical research personnel/clinical research units to coordinate and build opportunities for onsite shadowing.
4. In collaboration with the national and local team, evaluate programs and initiatives and conducting detailed analysis on program efficiency and student learning outcomes to inform program planning activities.
5. Foster cooperative working relationships with a wide variety of internal and external stakeholders to support initiatives
6. Develop, edit, and write content for marketing and communications materials for outreach activities and website.
7. Participates to the expansion of the training program by conducting outreach to other academic centres.
8. Collaborates with the team to develop, select and implement appropriate online content that supports course learning goals and objectives.
9. Create, manage & update online course content and assets on learning management system.
10. Develops toolboxes to guide mentorship and onsite shadowing
11. Manages the activities related to various training and educational programs for an organization, including supporting them in the start-up and maintenance of onsite mentorship and experiential learning or as hubs of training for the training program.
Website of the organization

Education / Experience
1. Bachelor's Degree or acceptable combination of equivalent experience.
2. Three (3) years of related experience, experience in a science or research environment preferred.
3. Experience organizing small or large professional or social in person or virtual events (particularly coordinating logistics, promotion, and communication).
4. Experience with LMS technology platforms, adult-learning principles or instructional design an asset.
5. Experience with technology platforms, including Zoom and various third-party event software programs (including LMS), Microsoft programs.
6. Demonstrated commitment to equity, diversity, and inclusion in practice.
7. Well-developed verbal, written communication skills and interpersonal skills.
8. Disciplined approach to planning and project execution with exceptional attention to accuracy and detail.
9. Proven problem-solving ability in managing concurrent projects under tight deadlines.
10. Ability to take initiative, show resourcefulness, and be attuned to the needs of various groups/individuals.
11. Experience with/interest in tools that facilitate reflection and learning within group settings, large and small, is an asset.
12. Bilingualism (English/French)
13. Ability and willingness to work occasional weekend and evening hours.
14. Ability and willingness to travel within Canada at least once per year to a maximum of 5 business days.
Additional information

**Status**: Temporary, one-year renewable. Full-time (35 hrs/week).

**Pay Scale**: Commensurate with experience and qualifications: $46,173 to $85,740

**Work Site**: Hybrid: In person at 2155, rue Guy, 5th floor 3 days / week, then telework.

Why work with us?
- 4-week vacation, 5th week after 5 years,
- Paid time off during the Holidays,
- Bank of 12 paid days (personal days and days for sickness or family ob



  • Montréal, Canada Fortrea Full time

    Clinical Trial Coordinator - Regulatory Hybrid (50% office-based / 50% remote) - Montreal, QC As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient...

  • Unit Manager

    6 days ago


    Montréal, Canada Centre universitaire de santé McGill Full time

    **Organization description** Le Centre universitaire de santé McGill (CUSM) est un centre hospitalier universitaire intégré, reconnu à l’échelle internationale pour l’excellence de ses programmes cliniques, de sa recherche et de son enseignement. Le CUSM a pour objectif d’assurer aux patients des soins fondés sur les connaissances les plus...


  • Montréal, Canada Fortrea Full time

    Clinical Trial Administrator, FSP Hybrid (50% client office-based / 50% remote) - Montreal, Quebec Must Commute to Client Office Two Days/Week We are seeking a Clinical Trial Administrator (CTA), an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The CTA is an administrative support role for...


  • Montréal, Canada Fortrea - Organic Full time

    Clinical Trial Administrator Montreal, QC Hybrid 50% client office / 50% home-based As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access...


  • Montréal, Canada Allphase Clinical Research Inc. Full time

    **Job Title**: FSP - Clinical Project Manager **Date**: May 17, 2024 **Location**: Montreal, QC **Remote**: Yes **Business Unit**: Health **Division**: Pharma - CRO - Do you want the opportunity to be embedded within big pharma? - Do you want to drive the strategy, planning and implementation of local research to address healthcare system gaps and ensure the...


  • Montréal, Canada Centre universitaire de santé McGill Full time

    **Organization description** Le Centre universitaire de santé McGill (CUSM) est un centre hospitalier universitaire intégré, reconnu à l’échelle internationale pour l’excellence de ses programmes cliniques, de sa recherche et de son enseignement. Le CUSM a pour objectif d’assurer aux patients des soins fondés sur les connaissances les plus...


  • Montréal, Canada Syneos Health Clinical Full time

    **Overview** **Vous êtes un expert extraverti, à la fois chercheur et communicatif, scientifique et social.** S’il y a une chose que votre préparation à l’obtention de votre diplôme d’études supérieures vous a apprise, c’est comment faire évoluer votre expertise rapidement et rester à l’avant-garde de votre domaine. Forger de nouvelles...


  • Montréal, Canada National Research Council Canada Full time

    Help bring research to life and drive your career forward with the National Research Council of Canada (NRC), Canada's largest research and technology organization. We are looking for an Health and Safety Programs Administrative Coordinator to support the new Clinical Trial Material Facility of the Human Health and Therapeutics Research Center (HHT). The...


  • Montréal, Canada Novartis Full time

    100,000. That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations (GCO) touches patients’ lives every day acting as a link between science and medicine. Envision the impact you could have! #GCO The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning, executing and reporting, (from...


  • Montréal, Canada Fortrea - Organic Full time

    Clinical Research Manager Remote - Montreal, Quebec As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across...


  • Montréal, Canada Centre universitaire de santé McGill Full time

    Job Description RESEARCH INSTITUTE OF THE MUHC The Research Institute of the McGill University Health Centre (RI-MUHC) is a world-renowned biomedical and hospital research centre. Located in Montreal, Quebec, the Institute is the research arm of the McGill University Health Centre (MUHC) affiliated with the Faculty of Medicine at McGill University. The...

  • Clinical Team Lead

    4 weeks ago


    Montréal, Canada Labcorp Full time

    **Clinical Team Lead** **Remote - Canada** **CRA and Lead Monitor Experience in Pharma and/or CRO Required** As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the...


  • Montréal, Canada Barrington James Full time

    Canadian based CRA needed for two sites one in Toronto the other in Montreal.MUST HAVE RECENT ONCOLOGY EXPERIENCE!!! T4 contract only. 0.25 FTE consultant needed for long term project. SummaryThe Clinical Research Associate plays a vital role in the Clinical Operations team. Through responsibilities like monitoring studies, reviewing data, and engaging with...


  • Montréal, Canada Fortrea Full time

    Clinical Research Manager Remote - Montreal, Quebec As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across...


  • Montréal, Canada National Research Council Canada Full time

    Join us in making biomedical innovations more accessible to Canadians. The new Biologics Manufacturing Centre is helping build Canada’s capacity to produce, access and supply vaccines and other biologics to advance Canada’s biomanufacturing sector and respond to public health emergencies. The Coordinator, Procedures & Training is playing a key role to...

  • Clinical Scientist

    1 month ago


    Montréal, Canada Fortrea - Organic Full time

    Clinical Scientist Support, FSP, Oncology - Remote - As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more...

  • Quality Assurance

    3 weeks ago


    Montréal, Canada NeuroRx Research Full time

    **The role**: The Quality Assurance / Quality Control Coordinator is part of NeuroRx’ QA Unit and is responsible for internal Quality Assurance (QA) monitoring activities as well as for Quality Control (QC) of MRI related data in our database. Duties of the Quality Assurance / Quality Control Coordinator include: - QC of quantitative measurement results...

  • Quality Assurance

    5 days ago


    Montréal, Canada NeuroRx Research Full time

    **The role**: The Quality Assurance / Quality Control Coordinator is part of NeuroRx’ QA Unit and is responsible for internal Quality Assurance (QA) monitoring activities as well as for Quality Control (QC) of MRI related data in our database. Duties of the Quality Assurance / Quality Control Coordinator include: - QC of quantitative measurement results...


  • Montréal, Canada Innovaderm Research Full time

    1 year replacement** Project Coordinator** The Project Coordinator offers administrative support to Project Managers and the project team at many stages during clinical studies projects. This role is perfect for you if: - You have an interest in project administration and clinical research; - You want to work in a collaborative environment; - You want to...


  • Montréal, QC, Canada Parexel Full time

    PXL is seeking a Clinical Research Manager (CRM) in Canada for one of our large FSP clients! This is a remote position with some travel. Oncology experience is preferred! The Clinical Research Manager (CRM) is responsible for the following: Primarily accountable for end-to-end performance and project management for assigned protocols in a country in...