11 meilleures offres (clinical research associate, brampton, on) (à pourvoir)

Clinical Research Coordinator (RN)
Cardio Health Inc. —Mississauga, ON
- De 30 $ à 35 $ de l’heure
- Temps partiel
- Microsoft Powerpoint
- Microsoft Word
- Certification RCR
- Assurance Dentaire
Postuler rapidement
Clinical Research Associate
Profound Medical —Mississauga, ON
- De 60 000 $ à 75 000 $ par an
- Temps plein
- Maîtrise
- Baccalauréat
- Amélioration continue
Global Study Leader
Jazz Pharmaceuticals —Mississauga, ON
- De 140 000 $ à 210 000 $ par an
- Microsoft Outlook
- Baccalauréat
- Gestion d'équipe
- Assurance Dentaire
- Assurance Vision
il y a 5 jours
MLS Laboratory Facilitator
Humber —Etobicoke, ON
- De 48,07 $ à 55,57 $ de l’heure
- Temps plein
- Expérience en laboratoire
- Maintenance
- Recherche
il y a 5 jours
Global Study Leader
Jazz Pharmaceuticals —Mississauga, ON
- De 140 000 $ à 210 000 $ par an
- Microsoft Outlook
- Baccalauréat
- Gestion d'équipe
- Assurance Dentaire
- Assurance Vision
il y a 5 jours
Senior Quality Assurance Associate
Sitero LLC —Mississauga, ON
- Temps plein
- Travail hybride
- Baccalauréat
- Congés payés
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QA Associate – Biologics - Eurofins CDMO Alphora, Inc.
Eurofins Canada BioPharma —Mississauga, ON
- 70 000 $ par an
- Embauche urgente
- Gestion de projet
- Baccalauréat
- Amélioration continue
- Jours fériés payés
- Assurance Invalidité
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R1558503 Directeur associé, Relations clientèle, gestionnaire de projet – Appareils connectés / Client Relationship Associate Director, Connected Devices PM (Clinical Research)
IQVIA —Mississauga, ON
- De 108 500 $ à 155 000 $ par an
- Temps plein
- Télétravail
- Microsoft Word
- Service à la clientèle
- Baccalauréat
Senior Clinical Trial Manager
Sitero LLC —Mississauga, ON
- Temps plein
- Travail hybride
- Expérience en gestion
- Baccalauréat
- Mentorat
- Congés payés
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Consultant associé, Services de conseil et d’analyse / Associate Consultant, Consulting & Analytics Services
IQVIA —Mississauga, ON
- De 72 500 $ à 120 900 $ par an
- Temps plein
- Microsoft Powerpoint
- Anglais
- Maîtrise
Consultant, Services de conseil et d’analyse / Consultant, Consulting & Analytics Services
IQVIA —Mississauga, ON
- De 97 500 $ à 147 500 $ par an
- Temps plein
- Microsoft Powerpoint
- Anglais
- Maîtrise

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Clinical Research Coordinator (RN)

Cardio Health Inc. -
Mississauga, ON

Postuler rapidement

Détails du poste

Permanent | Temps partiel | Temps plein
De 30 $ à 35 $ de l’heure

Profil recherché

Microsoft Powerpoint
Microsoft Word
Tenue de dossiers
Certification RCR
Prélèvement d'échantillons
Microsoft Excel
Signes vitaux
Administration de médicaments
Recherche clinique
Consentement éclairé
Tenue des dossiers
Électrocardiogramme
Étiquetage
Évaluation des patients
Compétences rédactionnelles
Logistique
Transcription
Membre de l'OIIO
Esprit d'analyse
Certificat de premiers soins de base
Saisie de données
Recrutement
Sens de l'organisation
Bonnes pratiques cliniques (BPC)
Procédures opératoires normalisées (PON)
Terminologie médicale
Compétences en communication
Expérience hospitalière
Coordination d'équipe

Description complète du poste

Cardio Health Clinical Trials (CHCT) is a site management organization with over a decade of experience in managing and conducting clinical trials across multiple therapeutic areas, specializing in Cardiovascular and Gastroenterology. With multiple investigator sites across Ontario, CHCT is committed to delivering personalized services with a team of qualified experts.

Position Summary

The Clinical Research Coordinator (CRC) plays a pivotal role in supporting, facilitating, and coordinating the day-to-day clinical trial activities under the direction of the Principal Investigator (PI). The CRC ensures the seamless execution of clinical trials while adhering to Good Clinical Practice (GCP) guidelines and regulatory standards. This role requires close collaboration with the Clinical Trial Manager, study sponsors, and institutional stakeholders.

Key Responsibilities

General Responsibilities

· Conduct clinical research studies in compliance with the study protocol, Good Clinical Practice (GCP), and CHCT Research SOPs.

· Participate in clinical trial activities, including pre-screening, screening, informed consent procedures, randomization, administration, vital signs and ECG recording, visit coordination, sampling, and scheduling.

· Maintain regulatory documentation and study-specific logs.

· Ensure timely and accurate transcription of data into source documents, paper case report forms, and electronic CRFs.

· Proficiently perform phlebotomy and handle biological sample processing.

· Travel to attend research and investigator meetings as required.

· Participate in monitoring visits, investigator meetings, site initiation visits, closeout visits, and audits.

· Manage package drops and pickups (e.g., Amazon, FedEx) to ensure study materials and samples are available and handled promptly.

Participant Engagement

· Recruitment: Identify, screen, and enroll eligible study participants while obtaining informed consent.

· Visit Coordination: Schedule patient visits as per protocol and maintain adherence to study timelines.

· Participant Interaction: Conduct study visits, assess adverse events, monitor safety, and collect biological samples.

Operational Support

· Study Compliance: Maintain accurate, up-to-date study binders and ensure adherence to regulatory requirements.

· Sample Handling: Collect, process, label, store, and ship biological specimens in line with protocol requirements.

· Equipment Oversight and Training:

o Conduct routine checks to ensure research equipment is functional.

o Train and operate trial-specific equipment, including cardiology diagnostic tools and specialized devices.

o Promptly report and address equipment-related issues.

· Package Management: Handle the pickup and delivery of study materials and samples efficiently.

Site Management

· Serve as a backup CRC at other CHCT sites as needed.

· Coordinate with team members to ensure seamless site operations and coverage.

QualificationsEducation

· You must hold a current certification of registration from the College of Nurses of Ontario and maintain membership with the RPNAO or RNAO.

Certifications

· Good Clinical Practice (GCP) certification (essential).

· Certifications from SOCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Professionals) are highly preferred.

· Phlebotomy certification is required.

· [NR1] CPR/First Aid certificate an asset

Experience

· 2-3 years of experience in clinical trials, research coordination, or related clinical roles (Phase 1-4 clinical trial experience is an asset).

· Infusion experience (e.g., IV insertion, IV drug administration, infusion monitoring)

· Experience in patient recruitment, informed consent, and patient visit coordination.

· Proficiency in biological sample collection, handling, and processing.

· Experience working in hospital or clinic settings for 2-3 years.

· Familiarity with electronic data capture systems and trial master files (TMFs).

Skills

· Experience in Physical Assessment: Proficient in medical terminology and capable of taking vital signs (BP, RR, temperature, etc.).

· Communication Skills: Excellent verbal and written communication for interactions with patients, sponsors, and research teams.

· Organizational Skills: Strong multitasking ability with exceptional attention to detail and accurate record-keeping.

· Regulatory Knowledge: Familiarity with Health Canada and FDA regulations relevant to clinical trials.

· Technical Proficiency: Competency in clinical trial management systems (CTMS) and MS Office Suite (Word, Excel, PowerPoint).

· Knowledge of IATA Shipping Regulations and Basic Laboratory Procedures: Ensures proper handling and transport of biological samples.

· Flexibility and Teamwork: Capable of working independently with minimal supervision and collaborating within a team environment.

· Problem-Solving and Analytical Skills: Ability to identify and resolve issues effectively.

Other Requirements

· Availability to work beyond standard business hours, including evenings and weekends, if required by the study protocol.

· Ability to travel between research sites when necessary.

· Access to reliable transportation for site visits and package deliveries.

· Adherence to professional appearance and conduct, following a business casual dress code or study-specific guidelines.

CPR/First Aid certificate an asset

Pay: $30.00-$35.00 per hour

Benefits:

Dental care
Extended health care

Application question(s):

Outline your clinical trial experience
Describe your experience with patient history taking
4. Provide examples of your organizational skills

Licence/Certification:

Registered Nurse License (required)

Willingness to travel:

75% (preferred)

Work Location: In person

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clinical research associate emplois - brampton, on

Clinical Research Coordinator (RN)

Clinical Research Associate

Global Study Leader

MLS Laboratory Facilitator

Global Study Leader

Senior Quality Assurance Associate

QA Associate – Biologics - Eurofins CDMO Alphora, Inc.

R1558503 Directeur associé, Relations clientèle, gestionnaire de projet – Appareils connectés / Client Relationship Associate Director, Connected Devices PM (Clinical Research)

Senior Clinical Trial Manager

Consultant associé, Services de conseil et d’analyse / Associate Consultant, Consulting & Analytics Services

Consultant, Services de conseil et d’analyse / Consultant, Consulting & Analytics Services

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