20 meilleures offres (clinical research associate, richmond hill, on) (à pourvoir)

Clinical Research Associate II
AbbVie —Toronto, ON
- De 81 000 $ à 131 000 $ par an
- Temps plein
- Télétravail
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
il y a 2 jours
Bilingual Sr. Clinical Research Associate
Alimentiv —Toronto, ON
- De 78 000 $ à 130 000 $ par an
- Temps plein
- Télétravail
- Bilingue
- Anglais
- Déplacements à prévoir
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Clinical Safety Data Associate
Everest Clinical Research —Markham, ON
- De 60 000 $ à 80 000 $ par an
- Médecine
- Doctorat
- Expérience en laboratoire
- Assurance Invalidité
- Assurance Dentaire
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Research Associate (SRI) - Evaluative Clinical Sciences - Temporary Full-time 2026-16467
Sunnybrook Health Sciences Centre —Toronto, ON
- Temporaire
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
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Clinical Research Associate - Canada
サイネオス・ヘルス —Toronto, ON
- Capacités de présentation
- Baccalauréat
- Déplacements à prévoir
il y a 13 jours
Research Coordinator, Paediatrics
Sinai Health —Toronto, ON
- De 32,71 $ à 40,85 $ de l’heure
- Temporaire
- Microsoft Word
- Microsoft Excel
- Microsoft Access
il y a 6 jours
Experienced Clinical Research Associate - Sponsor Dedicated
サイネオス・ヘルス —Toronto, ON
- Capacités de présentation
- Baccalauréat
- Déplacements à prévoir
- Plan d'actionnariat des employés
- Assurance Dentaire
Senior Research Associate (Permanent Full-Time)
VHA Home HealthCare —Toronto, ON
- De 70 000 $ à 87 000 $ par an
- Temps plein
- Travail hybride
- Doctorat
- Recherche
- Expérience administrative
- Programme d'Aide aux Employés
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il y a 14 jours
Research Associate (SRI) - Evaluative Clinical Sciences - Temporary Part-Time 2026-17895
Sunnybrook Health Sciences Centre —Toronto, ON
- Temporaire
- Doctorat
- Éducation
- Capacités de présentation
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il y a 1 jour
Associate Director, Ontario Tumour Bank
OICR —Toronto, ON
- De 131 000 $ à 146 300 $ par an
- Travail hybride
- PMP
- Recherche
- Maîtrise
il y a 2 jours
Scientist III
Unity Health Toronto —Toronto, ON
- De 82,40 $ à 122,20 $ de l’heure
- Temps plein
- Médecine
- Doctorat
- Recherche
- Assurance Invalidité
- Assurance Dentaire
il y a 14 jours
Research Associate (SRI) - Physical Sciences - Regular Full-Time 2026-17652
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Doctorat
- Ingénierie
- Recherche
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Sr. Clinical Operations Lead (Clinical Trial Manager)
Alimentiv —Toronto, ON
- De 78 000 $ à 130 000 $ par an
- Temps plein
- Télétravail
- Microsoft Office
- Baccalauréat
- Sens de l'organisation
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Associate Director, Medical Programs
Nucs AI —Toronto, ON
- Temps plein
- Travail hybride
- Expérience en laboratoire
- Recherche
- Maîtrise
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Research Associate (SRI) - Physical Sciences - Regular Full-time 2025-15843
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Doctorat
- Anglais
- Recherche
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Senior Research Associate
サイネオス・ヘルス —Toronto, ON
- Travail hybride
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
il y a 2 jours
Clinical Operations & Enablement Lead
Nucs AI —Toronto, ON
- Temps plein
- Travail hybride
- Maîtrise
- Capacités de présentation
- Baccalauréat
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Administrative Assistant (SRI) - Evaluative Clinical Sciences - Regular Full-time 2026-17356
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
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Guideline Development Methodologist 2026GDM006
Registered Nurses Association of Ontario —Toronto, ON
- 85 000 $ par an
- Heures supplémentaires
- Travail hybride
- Soins infirmiers
- Recherche
- Maîtrise
Postuler rapidement
Manager II, Study Management Associate (SMA)
AbbVie —Toronto, ON
- De 134 000 $ à 184 000 $ par an
- Temps plein
- Télétravail
- Expérience en gestion
- Esprit d'analyse
- Baccalauréat
il y a 9 jours

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

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Clinical Research Associate II

AbbVie -
Toronto, ON

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Détails du poste

Temps plein
De 81 000 $ à 131 000 $ par an
Il y a 2 jours

Profil recherché

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Microsoft Outlook
Microsoft Office
Esprit d'analyse
Sens de l'organisation
Permis de conduire

Description complète du poste

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

When choosing your career path, choose to be remarkable.

Job Description

To enable AbbVie’ s emergence as a world class R&D organization, the position anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol level execution of Clinical Site Management deliverables involving start-up, execution, and close-out of studies.

Key Responsibilities:

Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research.
Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase I to III studies in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs) and business processes.
Overviews the overall activities of site personnel over whom there is no direct authority and motivates/influences them to meet study objectives. proactively manages the site and ensures action plans are put into place as needed to ensure compliance. Ensures regulatory inspection readiness at assigned clinical sites.
Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
Ensures safety and protection of study subjects through compliance with the study monitoring plan, AbbVie SOPs, ICH Guidelines, and applicable regulations.
Trains study site personnel on the protocol and applicable regulatory requirements in collaboration with pertinent project team members.
Manages investigator payments as per executed contract obligations. Negotiates investigator/ hospital agreements with stakeholders. Maintain and complete own expense reports as per local and applicable guidelines.
Identifies, evaluates and recommends new/potential investigators/sites on an on going basis. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.

Qualifications

Appropriate tertiary qualification, health related (e.g., Medical, Scientific, Nursing) preferred.
Minimum of 2 years of clinically-related monitoring experience. Experience in on-site monitoring of investigational drug or device trials is required.
Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.
Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.
Familiarity with all aspects of study monitoring; data, drug accountability, documentation experience.
Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and follow work processes within the assigned function.
Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity. Ability to address study related clinical site issues with appropriate guidance and initiates and communicate corrective action as indicated. Ability to use functional expertise and exercise good judgment.
Demonstrated business ethics and integrity.
A minimum of 50% travel is required.
Proficient with Microsoft Office Suite (Outlook, PowerPoint, Excel, Word, etc.)
Must be at ease with technology (the use of various tools/systems to perform day-to-day tasks).
Travel required at least 50% of the time.

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

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clinical research associate emplois - richmond hill, on

Clinical Research Associate II

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Research Associate (SRI) - Physical Sciences - Regular Full-Time 2026-17652

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Administrative Assistant (SRI) - Evaluative Clinical Sciences - Regular Full-time 2026-17356

Guideline Development Methodologist 2026GDM006

Manager II, Study Management Associate (SMA)

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

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