20 meilleures offres (research assistant, canada remote) (à pourvoir)

Clinical Trial Assistant I
Everest Clinical Research —Markham, ON
- De 45 000 $ à 65 000 $ par an
- Télétravail
- Microsoft Office
- Expérience administrative
- Baccalauréat
- Assurance Invalidité
- Assurance Dentaire
Postuler rapidement
Clinical Trial IWRS Monitor (Overnight)
Everest Clinical Research —Markham, ON
- De 45 000 $ à 65 000 $ par an
- Télétravail
- En présentiel
- Assurance Invalidité
- Assurance Dentaire
Postuler rapidement
Research Associate
MD Analytics —Toronto, ON
- Temps plein
- Télétravail
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Postuler rapidement
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
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il y a 12 jours
Bilingual Sr. Clinical Research Associate
Alimentiv —Halifax, NS
- De 78 000 $ à 130 000 $ par an
- Temps plein
- Télétravail
- Bilingue
- Anglais
- Déplacements à prévoir
Postuler rapidement
Clinical Research Associate - Canada
Syneos - Clinical and Corporate - Prod —À domicile
- Temps plein
- Télétravail
- Capacités de présentation
- Baccalauréat
- Déplacements à prévoir
Associate, Research & Delivery (Portuguese Speaking)
Exiger —Toronto, ON
- De 45 000 $ à 60 000 $ par an
- Temps plein
- Travail hybride
- Anglais
- Recherche
- Esprit d'analyse
- Assurance Dentaire
- Assurance Vision
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Clinical Trial IWRS Monitor I
Everest Clinical Research —Markham, ON
- De 45 000 $ à 65 000 $ par an
- En présentiel
- Assurance Invalidité
- Assurance Dentaire
Postuler rapidement
Clinical Research Associate - Sponsor Dedicated - Bilingual
Syneos - Clinical and Corporate - Prod —À domicile
- Temps plein
- Télétravail
- Bilingue
- En présentiel
il y a 12 jours
Library Program Development Assistant
Region of Waterloo —Wilmot, ON
- De 30,26 $ à 34,24 $ de l’heure
- Temporaire
- Microsoft Office
- Déplacements à prévoir
- Compétences en informatique
- Travail à domicile
il y a 13 jours
Research Associate
Insightrix Research —Saskatoon, SK
- Travail hybride
- Microsoft Powerpoint
- Anglais
- Microsoft Office
Associate, Research & Delivery (English Speaking)
Exiger —Toronto, ON
- Travail hybride
- Espagnol
- Anglais
- Recherche
- Assurance Dentaire
- Assurance Vision
Postuler rapidement
Clinical Trial Associate 2
ICON Plc —Burlington, ON
- Temps plein
- Télétravail
- Baccalauréat
- Déplacements à prévoir
- Sens de l'organisation
- Assurance Invalidité
- Assurance Dentaire
il y a 13 jours
Lead Clinical Research Associate
PSI CRO —À domicile
- De 130 000 $ à 160 000 $ par an
- Temps plein
- Télétravail
- Anglais
- Microsoft Office
- Baccalauréat
Postuler rapidement
Bilingual Clinical Research Associate (CRA) - Montreal
Medpace, Inc. —Montréal, QC
- Temps plein
- Télétravail
- Bilingue
- Anglais
- Microsoft Office
- Congés payés
- Heures d'arrivée et de départ flexibles
Associate, Research & Delivery (Kurdish - Sorani Speaking)
Exiger —Toronto, ON
- De 45 000 $ à 60 000 $ par an
- Travail hybride
- Compétences rédactionnelles
- Recherche
- Esprit d'analyse
- Assurance Dentaire
- Assurance Vision
Postuler rapidement
Associate, Research & Delivery (Arabic Speaking)
Exiger —Toronto, ON
- De 45 000 $ à 60 000 $ par an
- Travail hybride
- Expérience en gestion
- Compétences rédactionnelles
- Recherche
- Assurance Dentaire
- Assurance Vision
Postuler rapidement
Bilingual, Freelance / Contractual Clinical Research Associate, Montreal,
Indero —À domicile
- Télétravail
- Microsoft Powerpoint
- Bilingue
- Microsoft Word
Postuler rapidement
11 h
Research Project Coordinator
University of New Brunswick —Fredericton, NB
- De 30,94 $ à 40,22 $ de l’heure
- Temps partiel
- Travail hybride
- Bilingue
- Informatique
- Anglais
- Heures d'arrivée et de départ flexibles
Education and Research Administrative Coordinator
Orthopaedic Surgery —Halifax, NS
- De 23,34 $ à 29,17 $ de l’heure
- Fins de semaine au besoin
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Congés payés
- Travail à domicile
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Clinical Trial Assistant I

Everest Clinical Research -
Markham, ON

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Détails du poste

Permanent
De 45 000 $ à 65 000 $ par an

Profil recherché

Microsoft Office
Expérience administrative
Baccalauréat
Compétences en informatique

Description complète du poste

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.

Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater New York City Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan.

Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.

Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s Everest.

To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as a Clinical Trial Assistant for our Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere in Canada in accordance with our Work from Home policy.

Job Accountabilities:

Interact with study Sponsors, investigational sites, vendors, and Everest functional groups to enable timely and high-quality operationalization of clinical trials in compliance with ICH-GCP and relevant local regulations.

Compile documentation for qualification of clinical sites. Support review of that documentation to ensure that those clinical sites comply with ICH-GCP and relevant local regulations.

Assist with preparation and submission of regulatory documents to responsible authorities and Institutional Review Boards/Ethics Committees.

Responsible for set-up, maintenance, and archival of studies in the Trial Master File (TMF) and Clinical Trial Management System (CTMS).

Establish, maintain, and archive files of essential documents from investigative sites and for inclusion in TMF. These files must be maintained in a fashion so that they are continuously available for inspection and completion for archive.

Assist with site identification, feasibility questionnaire development and distribution, and site selection.

Contribute to the development of Clinical Operations documents (i.e., Investigator Site File logs, newsletters, etc.) to facilitate the implementation and management of the clinical trial.

Collaborate with meeting planners and vendors to arrange for Investigator meetings, off-site client meetings (i.e., kick-off meetings), or internal departmental meetings.

Responsible for the shipment and tracking of trial documents (site binders, manuals, guides, etc.) and supplies, as needed.

Track monitoring plan compliance metrics (i.e., monitoring frequency and monitoring visit report submission/finalization). Issue reminders to monitoring team.

Distribute Suspected Unexpected Serious Adverse Reactions (SUSARs) to investigational sites and complete necessary tracking (acknowledgement of receipts, etc.).

Assist with the download of reports from Electronic Data Capture (EDC) systems and Interactive Web Response Systems (IWRS) to prepare summary of data for Project Managers/Clinical Trial Managers.

Maintain study portals, web sites, or newsletters.

Compile reports progress/status of investigational sites.

Assist with processing of vendor/site invoices and Investigator site payments.

Participate in the development and maintenance of and adhere to departmental Standard Operations Procedures (SOPs) and guidelines.

Collaborate with other team members to prepare, maintain, and complete training on study-specific and/or applicable Sponsor SOPs.

Support sites and internal Clinical Operations efforts to prepare for inspections and/or audits conducted either by Everest, Sponsors, or regulatory authorities.

Assist Clinical Operations team members with Requests for Proposals and other Clinical Operations tasks as needed.

Provide support for Clinical Operations and other functional areas as needed.

Qualifications:

Bachelor’s degree in Life Sciences or related field of study.

Excellent communication (both verbal and written) and computer skills.

Expert use of the Microsoft Office suite is essential.

Minimum of 1 year of experience in administrative support preferred.

Experience in managing and maintaining electronic TMFs.

Thorough knowledge of ICH-GCP guidelines and applicable regulations.

Ability to travel a maximum of 5% of working hours is required.

Benefits & Compensation:

We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus.

To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.everestclinical.com (http://www.everestclinical.com)

Estimated Salary Range: $45,000 - 65,000.

We thank all interested applicants, however, only those selected for an interview will be contacted.

Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.

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research assistant emplois - canada remote

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Clinical Trial IWRS Monitor (Overnight)

Research Associate

Research Assistant, Clinical Therapist

Bilingual Sr. Clinical Research Associate

Clinical Research Associate - Canada

Associate, Research & Delivery (Portuguese Speaking)

Clinical Trial IWRS Monitor I

Clinical Research Associate - Sponsor Dedicated - Bilingual

Library Program Development Assistant

Research Associate

Associate, Research & Delivery (English Speaking)

Clinical Trial Associate 2

Lead Clinical Research Associate

Bilingual Clinical Research Associate (CRA) - Montreal

Associate, Research & Delivery (Kurdish - Sorani Speaking)

Associate, Research & Delivery (Arabic Speaking)

Bilingual, Freelance / Contractual Clinical Research Associate, Montreal,

Research Project Coordinator

Education and Research Administrative Coordinator

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