Research Coordinator I Clinical Research Program
Unity Health Toronto —Toronto, ON
- Temporaire
- Télétravail
- Service à la clientèle
- Microsoft Office
- Bases de données
il y a 5 jours
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 12 jours
Clinical Research Coordinator
ClinSurge Research —Toronto, ON
- Temps plein
- Soins infirmiers
- Microsoft Office
- Baccalauréat
Postuler rapidement
Clinical Research Project Coordinator, iOUCH Pain Lab
SickKids —Toronto, ON
- Temporaire
- Expérience en laboratoire
- Bases de données
- Compétences en communication
11 h
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
Research Ethics Coordinator
OICR —Toronto, ON
- De 70 000 $ à 76 000 $ par an
- Travail hybride
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
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
Research Assistant 1 - Temerty Research Centre
CAMH —Toronto, ON
- De 23,64 $ à 29,15 $ de l’heure
- Temps plein
- Microsoft Powerpoint
- Bilingue
- Microsoft Word
il y a 2 jours
Research Assistant (SRI) - Evaluative Clinical Sciences - Regular Full-Time 2026-17599
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Microsoft Office
- Bases de données
- Baccalauréat
Postuler rapidement
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
Research Assistant II
Michael Garron Hospital —Toronto, ON
- Temporaire
- Traitement de texte
- Baccalauréat
- Sens de l'organisation
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
Postuler rapidement
Research Assistant I Dept of Surgery Research
Unity Health Toronto —Toronto, ON
- Temporaire
- Microsoft Powerpoint
- Microsoft Excel
- Traitement de texte
il y a 8 jours
Clinical Research Coordinator III (PK)
University Health Network —Toronto, ON
- De 84 779 $ à 105 968 $ par an
- Temps plein
- Microsoft Word
- Microsoft Excel
- Expérience en laboratoire
Postuler rapidement
il y a 12 jours
Research Ethics Coordinator - Research Institute
SickKids —Toronto, ON
- Temps plein
- Compétences rédactionnelles
- Recherche
- Baccalauréat
- Assurance Dentaire
il y a 6 jours
Clinical Research Assistant (SRI) - Centre for Clinical Trials - Regular Full-Time 2026-17750
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Postuler rapidement
il y a 1 jour
Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Casual 2026-16108
Sunnybrook Health Sciences Centre —Toronto, ON
- Maîtrise
- Psychologie
- Sens de l'organisation
Postuler rapidement
Research Coordinator - Temerty Centre Research
CAMH —Toronto, ON
- De 37,51 $ à 50,60 $ de l’heure
- Temps plein
- Microsoft Powerpoint
- Bilingue
- Traitement de texte
Research Assistant (SRI) - Evaluative Clinical Sciences - Regular Full-time 2026-17275
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Microsoft Office
- Maîtrise
- Esprit d'analyse
Postuler rapidement
Clinical Screening Coordinator (Regional West)
Centricity Research —Etobicoke, ON
- De 40 000 $ à 50 000 $ par an
- Temps plein
- Recherche
- Baccalauréat
- Jours fériés payés
- Assurance Dentaire
Postuler rapidement
Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2026-17216
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Microsoft Powerpoint
- Bilingue
- Microsoft Word
Postuler rapidement
Health Information Management Coordinator – Scheduling and Registration
SickKids Centre for Community Mental Health (CCMH) —Toronto, ON
- De 33,96 $ à 35,80 $ de l’heure
- Contrat
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
il y a 9 jours
Clinical Research Associate - Canada
サイネオス・ヘルス —Toronto, ON
- Capacités de présentation
- Baccalauréat
- Déplacements à prévoir
il y a 6 jours
Clinical Research Analyst
University Health Network —Toronto, ON
- 42,60 $ de l’heure
- Contrat
- Microsoft Excel
- Microsoft Access
- Microsoft Office
Postuler rapidement
il y a 9 jours

Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : clinical research coordinator (toronto, on)

En vous connectant à votre compte, vous acceptez les conditions d'utilisation, la politique relative aux fichiers témoins et la politique de confidentialité de Workopolis.

Research Coordinator I Clinical Research Program

Unity Health Toronto
Toronto, ON

Postuler dès maintenant

Détails du poste

Temporaire | Temps plein
Il y a 5 jours

Compétences

Utilisation d'un ordinateur
Service à la clientèle
Classement
Microsoft Office
Bases de données
Baccalauréat
Compétences en informatique
Compétences en communication

Description complète du poste

Research Coordinator I

The Research Institute is currently looking for a dynamic team player with excellent skills and experience in regulated clinical trials to fill an exciting new position as a Research Coordinator I.

Working within a newly established central clinical research unit, the position supports the efficient start-up, execution, and close-out of industry-sponsored clinical trials in compliance with Good Clinical Practice, Health Canada regulations, Division 5 of the Food and Drug Regulations, and institutional policies. The position will initiate new and support ongoing studies, including screening and recruiting eligible patients, obtaining informed consent, performing protocol-defined procedures, and accurately record study data in accordance with regulatory and quality standards.

The successful candidate will coordinate study activities across multiple investigators and clinical teams, standardizing workflows, supporting ethics and regulatory submissions, and ensuring accurate data collection and reporting. The position collaborates closely with sponsors and internal stakeholders to facilitate timelines, recruitment, and protocol adherence, while contributing to the development of streamlined processes and quality oversight within a growing centralized research infrastructure.

Additionally, the candidate will be responsible for providing administrative support including tracking and administering study related payments, maintaining appropriate inventory for study supplies, maintaining current lab licenses, freezer/drug logs and training certificates.

This position is full-time onsite with the option for occasional remote work.

Don’t meet every single requirement? Studies have shown that people in underrepresented communities are less likely to apply to jobs when they don’t meet every single qualification. We are dedicated to building an inclusive workplace, so if you’re excited about this role but your past experience doesn’t align perfectly, we still welcome you to apply.

Duties & Responsibilities:

Administrative Duties (50% of work time)

Creates trainings, manuals, e-learning content as needed.
Organizes, facilitates, and runs meetings with internal teams, and external stakeholders.
Facilitates the communication plan for internal and external stakeholders. Disseminates information as needed.
Ensures maintenance, collection, transcription, and entry of study related data, in accordance with hospital and privacy regulations.
General office duties e.g., filing, mailings, courier services, ensuring stocked and maintained inventory /supplies/equipment/software.
Designs all source documents (templates, tracking files, forms, guidance documents) for the collection, and management of information/data.
Organizes, sets up, and maintains equipment used in clinical research studies.
Provides high quality customer service experience when working with sponsors and external parties.

Research Specific Tasks (40% of work time)

Assists Principal Investigators and Research Program Manager in the initiation of new industry sponsored clinical trials and:
Coordinates and conducts screening, recruitment, and follow-up visits with participants.
Manages, prepares, and oversees monitors/audits.
Monitors, and controls research regulations, quality, and guidelines, including ethical (e.g., REB submissions), and safety protocols.
Writes and administers informed consent forms.
Arranges timely payments to participants.
Plans, organizes, directs, controls, and evaluates the activities and operations of research trials.
Liaises with multiple internal and external stakeholders at local and international levels, navigates stakeholder relationships, and responds proactively to anticipated challenges.
Helps develop processes, tools (workflow, Gantt charts), and resources to support team members, and projects.
Troubleshoots/solves logistical and technical obstacles.
Biological sample collection (Phlebotomy, dry blood spot testing etc.), processing and shipping according to Transportation of Dangerous Goods (TDG) and International Air Transport Association (IATA)
Maintains awareness of health and research news, events, and current high-profile research activities.

Day to day project and staff guidance tasks (10% of work time)

May train, coordinate, and/or delegate tasks (including overseeing quality control of submitted assignments) to Research Assistants, casual staff, students and internal/external collaborators.
May develop and implement policies, standards and procedures for the clinical trials and research operations in the department.

Performs cross functional and other duties as assigned and/or requested.

All staff are expected to carry out their assigned duties and responsibilities in a manner which prioritizes patient and employee safety, and confidentiality. Key accountabilities in this regard include:
Strict compliance with patient/employee confidentiality practices and policies.
Strict compliance with patient/employee safety practices and standards.
Appropriate identification, reporting and response to patient/employee confidentiality breaches in accordance with established policies and procedures.
Appropriate identification, reporting and response to patient/employee safety risks and incidents/events in accordance with established policies and procedures.

Qualifications:

Undergraduate Degree (Health Sciences preferred) and 2 years of relevant experience, OR demonstrable equivalent combination of specialized education and experience.
Experience with regulated clinical drug trials is preferred.
TCPS CORE 2, Good Clinical Practice and Health Canada Div 5 certificates are an asset. (Completed within first 2 weeks of hire)
Experienced phlebotomist with workshop certificate is an asset.
Completed a Clinical Research Academic Certificate Program is preferred
Clinical research professional designation is an asset (e.g., SOCRA, ACRP etc.).
Basic understanding of science, including applicable theories, frameworks, and models.
Excellent project coordination and problem solving skills.
Experience working with a diversity of stakeholders is an asset.
Empathy and ability to cope with emotionally difficult situations participants may be facing.
Basic computer skills with Microsoft Office experience, and database software (electronic data capture such as REDCap or Medidata).
Ability to work independently and as part of a team
Organization skills and ability to manage multiple projects simultaneously.
Excellent communication skills and strong interpersonal agility is an asset

Unity Health Toronto is committed to creating an accessible and inclusive organization. We strive to provide a recruitment process that is barrier-free and in compliance with the Accessibility for Ontarians with Disabilities Act (AODA) and the Ontario Human Rights Code. We understand that you may require an accommodation at any stage of the recruitment process. When you are contacted, please inform the Talent Acquisition Specialist and we will work with you to meet your accommodation needs. We want to emphasize that all accommodation requests are handled with the utmost confidentiality, respecting your privacy and dignity.

Postuler dès maintenant

Affinez votre recherche

clinical research coordinator emplois - toronto, on