18 meilleures offres (clinical research associate, markham, on) (à pourvoir)

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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Clinical Research Safety Associate
Everest Clinical Research-Can —Markham, ON
- De 60 000 $ à 85 000 $ par an
- Doctorat
- Microsoft Office
- Maîtrise
- Assurance Invalidité
- Assurance Dentaire
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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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Senior Research Coordinator
Baycrest —Toronto, ON
- De 66 021 $ à 82 526 $ par an
- Quart de jour
- Certification RCR
- Certificat de premiers soins de base
- Diplôme universitaire non requis
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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RESEARCH NURSE - RN
Unity Health Toronto —Toronto, ON
- Temporaire
- Soins Immédiats en Réanimation
- Baccalauréat
- Compétences en informatique
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
il y a 2 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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il y a 10 jours
Guideline Development Methodologist 2026GDM006
Registered Nurses Association of Ontario —Toronto, ON
- 85 000 $ par an
- Heures supplémentaires
- Travail hybride
- Soins infirmiers
- Recherche
- Maîtrise
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il y a 12 jours
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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il y a 8 jours
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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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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Sr. Medical Physicist - Medical Physics - Regular Full-Time - 2026-17624
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Baccalauréat
- Diplôme d'associé
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il y a 9 jours
Director, EVA Market Access
Cytel Inc —Toronto, ON
- Temps plein
- Médecine
- Expérience en gestion
- Doctorat
CRA I / CRA II - Sponsor Dedicated - Bilingual French and English (Home-based - Montreal, Quebec)
サイネオス・ヘルス —Toronto, ON
- Télétravail
- Bilingue
- Anglais
- Capacités de présentation
Lab Manager (SRI) - Physical Sciences - Regular Full-time 2026-16904
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Doctorat
- Ingénierie
- Gestion de projet
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Research Eng - Physicist (SRI) - Physical Sciences - Regular Full-time 2026-16670
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Informatique
- Ingénierie
- Expérience en laboratoire
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Clinical Safety Data Associate
Everest Clinical Research —Markham, ON
Develop study safety data review plans and maintain a standard set of data review checklists for clinical trial laboratory data, AEs, serious AEs (SAEs),…
De 60 000 $ à 80 000 $ par an
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Clinical Research Safety Associate
Everest Clinical Research-Can —Markham, ON
Support medical writing and clinical safety monitoring teams by performing quality control (QC) review of document deliverables, including clinical study…
De 60 000 $ à 85 000 $ par an
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Clinical Safety Data Associate

Everest Clinical Research -
Markham, ON

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Détails du poste

Permanent
De 60 000 $ à 80 000 $ par an

Profil recherché

Médecine
Doctorat
Expérience en laboratoire
Maîtrise
Gestion des données
Pharmacie

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 a committed, skilled, and customer-focused individual to join our winning team as a Clinical Safety Data Associate 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.

Key Accountabilities:

Develop study safety data review plans and maintain a standard set of data review checklists for clinical trial laboratory data, AEs, serious AEs (SAEs), medical events of special interests, concomitant medications, disease history, and early study termination due to AEs.

Perform safety data review according to the Safety Data Review Plan and review safety data in study database, including the review of laboratory data, AEs, SAEs, medical events of special interests, concomitant medications, disease history, and early study termination due to AEs. Follow up on issues identified during the review until they are resolved.

Coordinate with study Project Managers and Clinical Data Managers to maintain high-quality data collected in clinical trials. Document, report, and follow-up on all issues identified during the review in a timely manner.

Provide medical advice when required to the Clinical Data Managers for their work in reconciling SAEs.

Perform coding of AEs/medical histories/concomitant diseases using the MedDRA dictionary.

Perform coding of medications (e.g., concomitant medications, concomitant therapies, etc.) using the WHODrug dictionary.

Coordinate with Data Managers and ensure medical events and medications collected in study database are coded accurately and on a timely basis.

Participate in the trial protocol review and the review of trial Case Report Forms (CRFs) or eCRFs (electronic CRFs) and provide input to the requirements for accurate and consistent approaches in laboratory data collection.

Provide medical advice to the Clinical Data Manager with writing the Laboratory Edit Specifications, review the specifications to confirm accuracy, completeness, and ensure consistency across all studies. Review clinical trial laboratory data according to the standard review checklist(s) and interact with the Clinical Data Manager to resolve issues identified during the review.

Review and confirm laboratory normal ranges and units from both central laboratories and local laboratories. Interact with the Clinical Data Manager, Laboratory, or Clinical Site Monitor to ensure accuracy and consistency of the ranges and units.

Coordinate with and assist the Clinical Data Managers in managing local and central laboratory data and resolve related data issues.

Assist the Director of Medical Coding to ensure proper version control of the coding dictionaries and keep track of trial Sponsors’ requirements on coding dictionaries and ensure compliance on these requirements.

Participate in and contribute to Clinical Data Management initiatives.

Provide medical and coding support for programming and biostatistics activities and projects as required and needed.

Qualifications and Experience:

RN, M.D., M.Sc., or Ph.D. in Pharmacology or in health related science, Pharm.D., or equivalent education in relevant disciplines.

Two to three years’ experience in clinical trial data management, including medical coding and laboratory data management.

A broad knowledge in clinical trial safety data coding and management.

Demonstrated ability to effectively manage medical information; must communicate effectively, orally and in writing, with personnel on all professional and administrative levels; must be well organized and able to work independently and manage multiple projects/tasks appropriately.

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.

Estimated Salary Range: $60,000 - $80,000.

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)

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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clinical research associate emplois - markham, on

Clinical Safety Data Associate

Clinical Research Safety Associate

Bilingual Sr. Clinical Research Associate

Senior Research Coordinator

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

RESEARCH NURSE - RN

Experienced Clinical Research Associate - Sponsor Dedicated

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

Guideline Development Methodologist 2026GDM006

Sr. Clinical Operations Lead (Clinical Trial Manager)

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

Associate Director, Medical Programs

Research Associate (SRI) - Physical Sciences - Regular Full-time 2025-15843

Sr. Medical Physicist - Medical Physics - Regular Full-Time - 2026-17624

Director, EVA Market Access

CRA I / CRA II - Sponsor Dedicated - Bilingual French and English (Home-based - Montreal, Quebec)

Lab Manager (SRI) - Physical Sciences - Regular Full-time 2026-16904

Research Eng - Physicist (SRI) - Physical Sciences - Regular Full-time 2026-16670

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