14 meilleures offres (research coordinator, columbus) (à pourvoir)

Research Ethics Coordinator
Holland Bloorview Kids Rehabilitation Hospital —Toronto, ON
- Temps plein
- Recherche
- Microsoft Office
- Baccalauréat
il y a 4 jours
Research Coordinator
Baycrest —Toronto, ON
- De 58 386 $ à 72 983 $ par an
- Temps plein
- Maîtrise
- Baccalauréat
- Psychologie
Senior Research Coordinator
Baycrest —Toronto, ON
- De 66 021 $ à 82 526 $ par an
- Quart de jour
- Certification RCR
- Certificat de premiers soins de base
- Diplôme universitaire non requis
Clinical Research Coordinator
MyHealth Partners Inc. —Scarborough, ON
- De 100 000 $ à 120 000 $ par an
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Assurance Dentaire
- Congés payés
Postuler rapidement
Project Coordinator
McLean & Company —Toronto, ON
- Télétravail
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Postuler rapidement
il y a 7 jours
Clinical Research Coordinator
ClinSurge Research —Toronto, ON
- Temps plein
- Soins infirmiers
- Microsoft Office
- Baccalauréat
Postuler rapidement
Water Wastewater Compliance Coordinator
MISSISSAUGA'S OF SCUGOG ISLAND FIRST NATION —Port Perry, ON
- De 35,48 $ à 40,59 $ de l’heure
- Temps plein
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Postuler rapidement
Study Coordinator - Clinical Research
Pharma Medica Research Inc. —Toronto, ON
- De 50 000 $ à 55 000 $ par an
- Temps plein
- Anglais
- Maîtrise
- Baccalauréat
Postuler rapidement
il y a 13 jours
Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2026-17277
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
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Clinic Nurse & Research Coordinator, North York
Sentrex Distribution Inc. —North York, ON
- De 70 000 $ à 80 000 $ par an
- Quart de jour
- Certification RCR
- Microsoft Excel
- Esprit d'analyse
- Programmes de Bien-être
- Assurance Dentaire
Environmental Coordinator
Ledcor —Oshawa, ON
- De 80 100 $ à 106 800 $ par an
- Nuits au besoin
- Microsoft Office
- Construction et rénovation
- Compétences en communication
Project Coordinator: Ontario CLRI
Baycrest —Toronto, ON
- De 58 386 $ à 72 983 $ par an
- Temporaire
- Microsoft Excel
- PMP
- Recherche
Health and Wellness Coordinator
Baycrest —Toronto, ON
- De 66 021 $ à 82 526 $ par an
- Temps plein
- Certification RCR
- Expérience en laboratoire
- Maîtrise
Sample Coordinator
Rubicon Research —Concord, ON
- 36 608 $ par an
- Temps plein
- Microsoft Word
- Microsoft Excel
- Anglais
- Congés payés
Postuler rapidement

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Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : research coordinator (columbus)

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Research Ethics Coordinator

Holland Bloorview Kids Rehabilitation Hospital
Toronto, ON

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Détails du poste

Temps plein
Il y a 4 jours

Compétences

Recherche
Microsoft Office
Baccalauréat
Compétences en informatique
Compétences en communication

Description complète du poste

Join us in building a world of possibility!

Holland Bloorview Kids Rehabilitation Hospital is Canada’s largest pediatric rehabilitation hospital and is fully affiliated with the University of Toronto. It has ranked amongst Canada’s top 40 research hospitals for more than a decade. We offer an inspiring, inclusive, innovative, and collaborative work environment with competitive compensation and benefit packages and programs.

The Bloorview Research Institute (BRI), embedded within the hospital, is the only university-affiliated research institute in Canada dedicated to pediatric disability, and one of very few around the world. BRI’s vision is to be a global leader in transformative, equity-driven research dedicated to enabling personalized versions of a good life across the lifespan, for all individuals with childhood onset disabilities, acquired injuries and developmental differences, their families and communities.

The Position:

Reporting to the Manager, Office of Human Research Protections, the Coordinator, Research Ethics, is integral to the operations of the Research Ethics Office (REO) by supporting the Research Ethics Board (REB) and serving as the primary liaison between the REB and the research teams. The Coordinator, Research Ethics, is responsible for facilitating the research ethics review process, interpreting REB guidelines and practices governing human research participant protection, and the prompt processing of research ethics submissions to the Holland Bloorview REB through all stages of review, approval, and monitoring.

Additionally, the Coordinator, Research Ethics, will provide REB education along with the Research Ethics Office and REB Chair and Vice-Chair, and will be responsible for maintaining the REB website as well as the eREB system. The Coordinator, Research Ethics, supports the work of the REB Chair, Vice-Chair and REB members.

The Coordinator, Research Ethics will make a meaningful contribution to a wide range of projects and topics within BRI, providing outstanding opportunities for skills and knowledge development and professional growth.

In 2023, BRI celebrated the largest research expansion in its history, with the construction of an 11,000 square-foot research tower at 150 Kilgour Road, Toronto. The incumbent must be available to work on-site, with the possibility for remote work as operational needs allow.

Key Responsibilities:

Communication and Education

Educate, communicate and liaise effectively with the REB members, investigators, research/clinical staff, trainees and administrative staff throughout the hospital
Provide accurate and consistent information on ethical principles and REB standard operating procedures, and provide advice to research teams about REB process and requirements to assist research teams in meeting REB submission requirements as relevant to each submission
Maintain processes, and monitor practices to ensure research involving humans, with a particular emphasis on children and other vulnerable populations, complies with all regulations
Maintain the REB website as well as the eREB system
Oversee and coordinate student and intern placements within the REO, supervise and onboard students and interns, develop student and intern learning goals, oversee progress and ensure student program requirements are met

Administrative Functions

Coordinate and review all REB submissions including initial study approval, amendments, protocol deviations, unanticipated problems, adverse events, renewals, closures, researchers' responses to REB concerns and make recommendations for approval or need for revision
Assists with the preparation of REB meeting packages
Work with the REB Chair, Vice-Chair and Research Ethics Office to ensure compliance with relevant regulations, guidelines and policies throughout ethics review, approval and monitoring process
Provide accurate and complete documentation of REB discussions and decisions
Coordinate the maintenance of electronic and paper files to ensure timely and accurate record keeping; responsible for appropriate archiving of files (as required)
Assist in the development, implementation and communication of standard operating procedures, guidance documents and forms relating to the REB and REO
Maintain and update electronic databases and activity reports
Assist in Compiling, analyzing and interpreting REB/REO metrics for reporting purposes

Specialized Skills

Demonstrated competency in Tri-Council Policy Statement (TCPS2): Ethical Conduct for Research Involving Humans and International Conference on Harmonization – Good Clinical Practice (ICH-GCP), Health Canada and FDA Regulations
Possess a working knowledge of health research methodology

Qualifications:

Bachelor's degree in bioethics, life sciences, or a health-related field is required
Minimum of 2 years of work experience in a clinical research environment is required
Previous work experience within a research ethics office is strongly preferred
Adept at working in a fast-paced, rapidly changing academic research environment
Excellent communication, judgment, interpersonal skills, analytic skills, problem-solving skills and consultative skills
Demonstrated ability to work collaboratively within a team as well as independently
Computer proficiency, especially MS Office applications
Demonstrated ability to handle highly sensitive confidential information with tact, discretion and respect
Must be resourceful
Ability to set priorities and manage a busy work schedule
Background in childhood disability is an asset
Previous experience with CTO is an asset
Experience with electronic REB application system (e.g. Infonetica) is an asset

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Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2026-17277

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Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : research coordinator (columbus)

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