20 meilleures offres (research participant study, toronto, on) (à pourvoir)

Clinical Research Coordinator
North York Research Inc. —North York, ON
- À partir de 23 $ de l’heure
- Embauche urgente
- Expérience en laboratoire
- Pas d'expérience requise
- Microsoft Office
Postuler rapidement
il y a 3 jours
Research Analyst - TAY Cohort Study
CAMH —Toronto, ON
- De 27,95 $ à 37,28 $ de l’heure
- Temps plein
- Microsoft Powerpoint
- Bilingue
- Microsoft Word
il y a 5 jours
Research Associate, Health Technology Evaluation
University Health Network —Toronto, ON
- De 37,85 $ à 47,31 $ de l’heure
- Contrat
- Analyse de données
- Recherche
- Maîtrise
Postuler rapidement
il y a 8 jours
Senior Analyst, Real Estate Development
Fiera Capital —Toronto, ON
- De 90 000 $ à 110 000 $ par an
- Temps plein
- Travail hybride
- Bilingue
- Microsoft Excel
- Anglais
Senior Product Manager
InfoTrack Canada —Toronto, ON
- De 120 000 $ à 140 000 $ par an
- Temps plein
- Travail hybride
- Bilingue
- Anglais
- Capacités de présentation
Postuler rapidement
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
Research Assistant 2 - General Adult Division Research
CAMH —Toronto, ON
- De 26,80 $ à 33,05 $ de l’heure
- Temps partiel
- Bilingue
- Anglais
- Recherche
il y a 6 jours
Research Assistant I Anaesthesia Research
Unity Health Toronto —Toronto, ON
- De 27,13 $ à 33,91 $ de l’heure
- Temporaire
- Recherche
- Microsoft Office
- Baccalauréat
il y a 1 jour
Research Analyst - Institute for Mental Health Policy Research
CAMH —Toronto, ON
- De 27,95 $ à 37,28 $ de l’heure
- Temps plein
- Bilingue
- Analyse de données
- Anglais
Research Associate
SE Health —Markham, ON
- De 69 000 $ à 87 000 $ par an
- Temporaire
- Travail hybride
- Analyse de données
- Recherche
- Maîtrise
Research Coordinator I Map ESTIMATE Lab
Unity Health Toronto —Toronto, ON
- De 39,11 $ à 48,89 $ de l’heure
- Temporaire
- Travail hybride
- Expérience en gestion
- Microsoft Office
- Bases de données
3 h
Research Coordinator I RADIS Research and Simulation Lab
Unity Health Toronto —Toronto, ON
- De 39,11 $ à 48,89 $ de l’heure
- Temporaire
- Informatique
- Informatique
- Ingénierie
il y a 6 jours
Research Coordinator - Forensic Research
CAMH —Toronto, ON
- De 37,51 $ à 50,60 $ de l’heure
- Temps partiel
- Microsoft Powerpoint
- Bilingue
- Traitement de texte
il y a 6 jours
Research Coordinator I Pediatric Research Urban Child Health
Unity Health Toronto —Toronto, ON
- De 39,11 $ à 48,89 $ de l’heure
- Temporaire
- Anglais
- Recherche
- Microsoft Office
il y a 7 jours
Research Assistant, Clinical Therapist
Ontario Institute for Studies in Education —Toronto, ON
- De 40 $ à 65 $ de l’heure
- Temps partiel
- Travail hybride
- Maîtrise
- Expérience auprès des enfants
- Éducation
- Travail à domicile
- Heures d'arrivée et de départ flexibles
Postuler rapidement
il y a 12 jours
Research Coordinator
Baycrest —Toronto, ON
- De 58 386 $ à 72 983 $ par an
- Temps plein
- Maîtrise
- Baccalauréat
- Psychologie
Clinical Research Associate II (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-Time 2026-17987
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Expérience en laboratoire
- Microsoft Office
- Bases de données
- Congés payés
Postuler rapidement
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
Research Analyst - Pre-Clinical Research
CAMH —Toronto, ON
- De 27,95 $ à 37,28 $ de l’heure
- Temps plein
- Informatique
- Ingénierie
- Recherche
Research Associate (SRI) - Evaluative Clinical Sciences - Temporary Full-time 2026-16467
Sunnybrook Health Sciences Centre —Toronto, ON
- Temporaire
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Postuler rapidement

Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : research participant study (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 SimplyHired.

Découvrir les offres d'emploi dans d'autres lieux

research participant study jobs near toronto, on

Research Coordinator (Toronto, ON) : offres d'emploi

Mental Health Therapist (Toronto, ON) : offres d'emploi

Research Analyst (Toronto, ON) : offres d'emploi

Clinical Research Assistant (Toronto, ON) : offres d'emploi

Senior Product Manager (Toronto, ON) : offres d'emploi

Clinical Evaluator (Toronto, ON) : offres d'emploi

Research Associate (Toronto, ON) : offres d'emploi

Clinical Research Associate (Toronto, ON) : offres d'emploi

Clinical Therapist (Toronto, ON) : offres d'emploi

Research Assistant (Toronto, ON) : offres d'emploi

Clinical Research Coordinator (North York, ON) : offres d'emploi

Real Estate Analyst (Toronto, ON) : offres d'emploi

Construction Coordinator (Ontario) : offres d'emploi

Operations Coordinator (Edmonton, AB) : offres d'emploi

Research Coordinator (Hamilton, ON) : offres d'emploi

Research (Winnipeg, MB) : offres d'emploi

Research Coordinator (London, ON) : offres d'emploi

Research Coordinator (University Of British Columbia (vancouver Campus), BC) : offres d'emploi

Research Coordinator (Manitoba) : offres d'emploi

Part Time Store Associate , Marshalls (Windsor, ON) : offres d'emploi

Clinical Research Coordinator

North York Research Inc. -
North York, ON

Postuler rapidement

Détails du poste

Temps plein
À partir de 23 $ de l’heure
Il y a 3 jours

Profil recherché

Audit financier
Phlébotomie
Expérience en laboratoire
Pas d'expérience requise
Google Cloud Platform
Microsoft Office
Saisie de données

Description complète du poste

Company Overview

North York Research Inc. is the high-volume Clinical Research Division of North York Dermatology Clinic.

We conduct Phase II–IV clinical trials across multiple dermatologic conditions, including atopic dermatitis, psoriasis, vitiligo, chronic hand eczema, acne vulgaris, prurigo nodularis, lichen simplex chronicus, urticaria, discoid lupus erythematosus, and hidradenitis suppurativa.

Our site operates in a fast-paced, multi-study environment, supporting leading pharmaceutical sponsors and CROs.

Role Overview

This is a hands-on, operational Clinical Research Coordinator role.

We are seeking an experienced CRC who can independently coordinate active dermatology clinical trials within a regulated Canadian clinical research environment.

The successful candidate must demonstrate:

True study ownership
Experience managing active clinical trials independently
Familiarity with Canadian REB processes
Strong working knowledge of GCP
Ability to manage real-world site operations, competing priorities, and sponsor/CRO expectations

This role is intended for individuals seeking long-term CRC-level responsibility. We are particularly interested in candidates seeking long-term growth and continued development within site-level clinical research operations.

Work Schedule

Full-time, on-site position
Core clinic hours: 8:00 AM – 5:00 PM
Flexibility required based on patient visits, monitoring visits, sponsor requests, and study needs

Key Responsibilities

Study Coordination & Ownership

Independently coordinate dermatology clinical trials from start-up through close-out
Ensure protocol adherence, visit execution, and inspection-ready documentation
Serve as a primary site contact for sponsors, CROs, CRAs, and monitors
Prepare for, host, and follow up on monitoring visits, remote reviews, audits, and close-out visits
Track study progress, outstanding action items, visit windows, and sponsor deliverables

Regulatory & Ethics Oversight

Manage REB submissions, amendments, renewals, safety submissions, and correspondence
Maintain complete and inspection-ready regulatory binders and site files
Maintain accurate delegation documentation and training records
Ensure informed consent is obtained, documented, and maintained according to REB-approved procedures
Identify, document, and escalate protocol deviations as required

Data & Systems Management

Complete timely and accurate data entry in EDC systems
Resolve queries independently and within sponsor/CRO timelines
Maintain accurate study tracking in CTMS and internal site trackers
Follow up with sponsors, CROs, and monitors on outstanding data, regulatory, and operational items

Clinical & Laboratory Oversight

Coordinate participant visits and subject flow
Ensure study assessments are completed according to protocol requirements
Oversee lab processing, shipment, documentation, and issue resolution
Maintain chain of custody, temperature logs, sample tracking, and lab-related source documentation
Identify and escalate lab, visit, or documentation issues promptly

Team & Site Collaboration

Provide guidance and oversight to Research Assistants involved in study activities
Communicate clearly with investigators, site staff, sponsors, CROs, and monitors
Escalate operational, compliance, or patient-related concerns appropriately
Contribute to workflow improvement, site quality, and inspection readiness

Required Qualifications

Applicants must demonstrate:

Minimum 1 year of hands-on Clinical Research Coordinator experience in regulated clinical trials. Candidates should be capable of independently managing core CRC responsibilities.
Experience coordinating regulated clinical trials in Canada
Familiarity with Canadian REB processes
Strong working knowledge of GCP
Independent ownership of:
Study conduct and visit execution
Monitoring visit preparation and follow-up
Protocol deviation identification and documentation
EDC data entry and query resolution
CTMS or study tracking systems
Regulatory binder/site file maintenance
Strong attention to detail, accountability, follow-through, and operational judgment
Proficiency with Microsoft Office and/or Google Workspace

Preferred Qualifications

Direct dermatology clinical trial experience
Experience with Phase II–IV studies
Phlebotomy experience
Lab processing and sample shipment experience
Audit, inspection, or monitoring visit exposure
Interest in continued growth within CRC-level clinical trial operations

Role Structure

Reports to: Clinical Research Supervisor and Investigator / Research Director
Autonomy: High; expected to manage assigned studies independently
Pace: Fast-paced, structured, accountability-driven, multi-study environment
Growth: Expanded study ownership based on demonstrated performance

Application Instructions

Resume only.

Applications that do not demonstrate independent CRC-level experience in regulated clinical trials will not be considered.

Pay: From $23.00 per hour

Application question(s):

Q1. Independent CRC Role

Have you functioned independently as the primary Clinical Research Coordinator on at least one study?
☐ Yes
☐ No

Q2. CRC Experience

How long have you worked specifically as a Clinical Research Coordinator in Canada?
☐ Less than 1 year
☐ 1–2 years
☐ 3–4 years
☐ 5+ years

Q3. REB & Ethics Responsibility

Which best describes your experience with Canadian REB/ethics submissions?
☐ Independently managed submissions and amendments
☐ Assisted under supervision
☐ No experience

Q4. Informed Consent

What was your level of involvement in informed consent?
☐ Independently conducted and documented consent
☐ Assisted under supervision
☐ No involvement

Q5. Study Load Responsibility

At your previous site, how many studies were you actively coordinating at the same time as the primary CRC?
☐ 1–2
☐ 3–5
☐ 6–8
☐ 8+

Q6. Monitoring Visits

Which best describes your role during monitoring visits?
☐ I prepare independently, host visits, and complete follow-up
☐ I assist another coordinator
☐ I do not participate

Q7. EDC Responsibility

Which best describes your EDC experience?
☐ Independent data entry, query resolution, and review
☐ Data entry only
☐ No EDC experience

Q8. Dermatology Trials

What is your experience with dermatology clinical trials?
☐ Independently coordinated dermatology trials
☐ Assisted only
☐ No dermatology experience

Q9. Clinical Skills

Which of the following have you performed in a clinical research setting? (Select all that apply)
☐ Phlebotomy
☐ ECG acquisition
☐ Vitals collection
☐ None of the above

Q10. Visit & Workflow Volume

On a typical clinic day, how many patient visits were you directly responsible for managing?
☐ 1–3
☐ 4–6
☐ 7–10
☐ 10+

Q11. SMO Experience (Asset)

Have you worked with or at a Site Management Organization (e.g., Probity Medical Research)?
☐ Yes
☐ No

Q12. Availability

What is your earliest available start date?
☐ Immediately
☐ Within 2 weeks
☐ Within 1 month
☐ More than 1 month

Q13. Delegation & RA Oversight

Have you worked with Research Assistants supporting your studies (e.g., lab prep, scheduling, source prep)?
☐ Yes — I delegated and reviewed their work
☐ Yes — but I did not oversee them
☐ No

Q14. Protocol Deviation Handling

When a protocol deviation occurs, what has been your typical role?
☐ I identify, document, and follow through to resolution
☐ I report to someone else to manage
☐ I have not handled deviations

Work Location: In person

Postuler rapidement

Affinez votre recherche

research participant study emplois - toronto, on

Clinical Research Coordinator

Research Analyst - TAY Cohort Study

Research Associate, Health Technology Evaluation

Senior Analyst, Real Estate Development

Senior Product Manager

Clinical Research Assistant (SRI) - Centre for Clinical Trials - Regular Full-Time 2026-17750

Research Assistant 2 - General Adult Division Research

Research Assistant I Anaesthesia Research

Research Analyst - Institute for Mental Health Policy Research

Research Associate

Research Coordinator I Map ESTIMATE Lab

Research Coordinator I RADIS Research and Simulation Lab

Research Coordinator - Forensic Research

Research Coordinator I Pediatric Research Urban Child Health

Research Assistant, Clinical Therapist

Research Coordinator

Clinical Research Associate II (SRI) - Odette Cancer Centre Clinical Trials - Regular Full-Time 2026-17987

Research Assistant (SRI) - Evaluative Clinical Sciences - Regular Full-time 2026-17275

Research Analyst - Pre-Clinical Research

Research Associate (SRI) - Evaluative Clinical Sciences - Temporary Full-time 2026-16467

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

Related Searches

Découvrir les offres d'emploi dans d'autres lieux

Outils pour les chercheurs d'emploi

Outils Employeurs

Parcourir

Garder le contact