9 meilleures offres (clinical trial coordinator, scarborough, on) (à pourvoir)

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
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Study Coordinator - Clinical Research
Pharma Medica Research Inc. —Toronto, ON
- De 50 000 $ à 55 000 $ par an
- Temps plein
- Anglais
- Maîtrise
- Baccalauréat
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Clinical Research Quality and Training Coordinator
ClinSurge Research —Toronto, ON
- Temps plein
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
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il y a 1 jour
Clinical Research Coordinator
Centricity Research —Toronto, ON
- De 55 000 $ à 62 500 $ par an
- Temps plein
- Baccalauréat
- Terminologie médicale
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il y a 3 jours
Coordinator, Quality Assurance and Education - Human Research Protections Program - Regular Full-Time 2026-17631
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
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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
il y a 3 jours
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 9 jours
Clinical Research Coordinator III (Nurse)
University Health Network —Toronto, ON
- De 84 779 $ à 105 968 $ par an
- Contrat
- Expérience en laboratoire
- Baccalauréat
- Compétences en communication
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il y a 11 jours
Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Casual 2026-16108
Sunnybrook Health Sciences Centre —Toronto, ON
- Maîtrise
- Psychologie
- Sens de l'organisation
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Clinical Research Assistant
Everest Clinical Research —Markham, ON
May assist with hardcopy and electronic archiving of clinical trial documents, including filing within a Trial Master File, according to established document…
De 45 000 $ à 70 000 $ par an
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Research Assistant I Anaesthesia Research
Unity Health Toronto —Toronto, ON
This entry-level position provides an excellent opportunity to develop practical clinical research skills within a large academic research program and offers…
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Clinical Research Coordinator
MyHealth Partners Inc. —Scarborough, ON
Bachelor's degree in health-related field required, Master's degree is an asset. Financial duties relating to clinical trial activities including budget…
De 100 000 $ à 120 000 $ par an
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Clinical Research Quality and Training Coordinator
ClinSurge Research —Toronto, ON
Bachelor's degree in Business Administration, Education, Human Resources, Quality Management, or a related field (preferred).
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il y a 1 jour

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Clinical Research Coordinator

MyHealth Partners Inc. -
Scarborough, ON

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Détails du poste

Permanent
De 100 000 $ à 120 000 $ par an

Profil recherché

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Phlébotomie
Microsoft Office
Maîtrise
Baccalauréat
Compétences en informatique
Compétences en communication

Description complète du poste

About WELL Health Diagnostic Centres

WELL Health Diagnostic Centres is the largest operator of independent diagnostic health facilities in Ontario. More than 15,000 Ontario healthcare providers refer their patients to WELL Health Diagnostic Centres’ 50+ accredited locations for OHIP-covered cardiology, imaging, women’s health, telehealth, and sleep diagnostic services.

WELL Health Diagnostic Centres is a top employer of choice! We are proud to be recognized year after year as an industry leader, earning distinctions such as Canada’s Best Managed Companies, Great Place to Work®, Canada’s Top Growing Companies from The Globe and Mail, and the Consumer Choice Award.

Why Join WELL Health Diagnostic Centres?

Compassionate & Connected Healthcare: Join a team of 1,000+ healthcare professionals across Canada dedicated to delivering excellent patient care while upholding the highest clinical standards.
Employee Wellness: We support your overall work-life balance and offer full access to our group medical benefits and external wellness platforms to support you in thriving both personally and professionally.
Competitive & Comprehensive Compensation: Enjoy competitive pay, extended health and dental benefits, paid time off, and exclusive perks through Perkopolis with 5,000+ discounts.
Grow with a Leading Organization: With 60+ clinics across Canada and upcoming rapid expansion, you’ll have the opportunity to advance your skills and build a meaningful career.
Collaborative & Supportive Culture: Work in a team-oriented environment with strong leadership, mentorship opportunities, continuing education support, training and development support, internal mobility, and clear pathways for career growth.

Visit us at https://welldiagnostics.ca (https://welldiagnostics.ca)

Responsibilities will include but are not limited to:

Function as part of a interdisciplinary, patient-focused team of professionals to ensure smooth and efficient facilitation of clinical trial activities
Manage day-to-day activities of a clinical trial including screening and recruiting eligible participants, obtaining informed consent, collecting and managing study data and ensuring compliance with protocols and regulatory guidelines
Initiate, manage, and coordinate submissions to Research Ethics Board and contracts for Legal Review
Communicate with internal hospital departments to complete impact assessments, facilitate departmental research agreements and obtain institutional approvals
Financial duties relating to clinical trial activities including budget development, invoicing and study-related patient reimbursements
Establish, maintain and complete all essential documents in Investigator Site File (ISF) ensuring adherence to regulatory requirements
Coordinate patient follow-up visit schedules as per study protocol and execution of all aspects of study visits including protocol specific assessments such as obtaining patient vitals, electrocardiograms and sample collection/processing
Report Adverse Events/Serious Adverse Events as per protocol and sponsor requirements
Liaise with sponsors as required
Prepare for monitoring visits, audits and inspections
Provide support to Site Operations Manager in tasks including but not limited to collection/reporting of institutional Key Performance Indicators, establishing clinical trial workflows and tools/templates
Support implementation of a clinical trial management system

Qualifications:

Minimum 3 years of clinical research experience in a hospital setting or clinical research setting
Bachelor's degree in health-related field required, Master's degree is an asset
Recognized certification in clinical research (ACRP or SOCRA) is an asset
Training and experience or willingness to be trained in Phlebotomy/Venipuncture practice required
Demonstrated knowledge of research regulations and guidelines (ICH/GCP, Health Canada, Tri-Council Policy, Declaration of Helsinki, etc.)
Proficiency in computer skills (Microsoft Office: Word, Excel, PowerPoint, Adobe)
Experience with Clinical Trial Management Systems and Electronic Data Capture systems an asset
Strong oral and written communication skills
A "can do" attitude: Flexibility to work in a complex environment with ability to multitask and prioritize to meet deadlines
Demonstrates initiative and the ability to work effectively both independently and as part of a team

WELL Health Diagnostic Centres does not use artificial intelligence-assisted tools as part of the recruitment process.

This role is for an existing vacancy. The expected hiring range for this role is from $100,000 to $120,000 annually. Final compensation is determined based on market location, job-related knowledge, skills, experience level, and internal equity. Candidates with significantly more experience may be considered at a higher level with adjusted compensation for certain roles.

WELL Health Diagnostic Centres welcomes and encourages applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.

WELL Health Diagnostic Centres is an equal opportunity employer. If you require accommodation for a disability at any stage of the recruitment process, please notify Human Resources.

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clinical trial coordinator emplois - scarborough, on

Clinical Research Coordinator

Study Coordinator - Clinical Research

Clinical Research Quality and Training Coordinator

Clinical Research Coordinator

Coordinator, Quality Assurance and Education - Human Research Protections Program - Regular Full-Time 2026-17631

Research Coordinator I Map ESTIMATE Lab

Research Coordinator I RADIS Research and Simulation Lab

Clinical Research Coordinator III (Nurse)

Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Casual 2026-16108

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