20 meilleures offres (clinical trial manager, remote) (à pourvoir)

Clinical Research Assistant
Everest Clinical Research —Markham, ON
- De 45 000 $ à 70 000 $ par an
- Microsoft Office
- Maîtrise
- Baccalauréat
- Assurance Invalidité
- Assurance Dentaire
Postuler rapidement
Principal Data Manager I
Everest Clinical Research —Markham, ON
- De 130 000 $ à 165 000 $ par an
- Télétravail
- Maîtrise
- Capacités de présentation
- Baccalauréat
- Assurance Invalidité
- Assurance Dentaire
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Clinical Trial Manager II / Gestionnaire d’essais cliniques II, Canada, remote
Indero —À domicile
- Télétravail
- Microsoft Powerpoint
- Microsoft Word
- Soins infirmiers
- Assurance Dentaire
- Travail à domicile
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5 h
Sr. Clinical Operations Lead (Clinical Trial Manager)
Alimentiv —London, ON
- De 78 000 $ à 130 000 $ par an
- Temps plein
- Télétravail
- Microsoft Office
- Baccalauréat
- Sens de l'organisation
Postuler rapidement
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
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
Clinical Project Manager
TruMinds Technology Inc —À domicile
- De 80 000 $ à 90 000 $ par an
- Temps plein
- Télétravail
- Soins infirmiers
- Maîtrise
- Gestion de projet
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Clinical Research Associate - Canada
Syneos - Clinical and Corporate - Prod —À domicile
- Temps plein
- Télétravail
- Capacités de présentation
- Baccalauréat
- Déplacements à prévoir
Clinical Data Manager
Everest Clinical Research —Markham, ON
- De 60 000 $ à 90 000 $ par an
- Télétravail
- Doctorat
- Maîtrise
- Bases de données
- Assurance Invalidité
- Assurance Dentaire
Postuler rapidement
Clinical Trials Proposal Manager
PSI CRO —Mississauga, ON
- De 90 000 $ à 120 000 $ par an
- Temps plein
- Télétravail
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Postuler rapidement
Clinical Data Management Specialist
Everest Clinical Research —Markham, ON
- De 45 000 $ à 70 000 $ par an
- Télétravail
- Maîtrise
- En présentiel
- Assurance Invalidité
- Assurance Dentaire
Postuler rapidement
Clinical Data Coordinator
Alimentiv —London, ON
- De 41 000 $ à 68 000 $ par an
- Temps plein
- Télétravail
- Compétences en communication
Postuler rapidement
Bilingual Sr. Clinical Research Associate
Alimentiv —Ottawa, ON
- De 78 000 $ à 130 000 $ par an
- Temps plein
- Télétravail
- Bilingue
- Anglais
- Déplacements à prévoir
Postuler rapidement
Gestionnaire d'essais cliniques II, IQVIA Biotech/Clinical Trial Manager II, IQVIA Biotech
IQVIA —Ottawa, ON
- De 116 300 $ à 193 800 $ par an
- Temps plein
- Télétravail
- Gestion de projet
- Baccalauréat
Senior Clinical Data Manager
Everest Clinical Research —Markham, ON
- De 90 000 $ à 130 000 $ par an
- Télétravail
- Maîtrise
- En présentiel
- Assurance Invalidité
- Assurance Dentaire
Postuler rapidement
Manager, Clinical Data Management
Everest Clinical Research —Markham, ON
- De 140 000 $ à 170 000 $ par an
- Télétravail
- Baccalauréat
- En présentiel
- Assurance Invalidité
- Assurance Dentaire
Postuler rapidement
Senior Clinical Data Manager - Remote, Canada based
Fortrea —À domicile
- De 84 000 $ à 145 000 $ par an
- Temps plein
- Télétravail
- Anglais
- Baccalauréat
- Diplôme universitaire non requis
- Assurance Invalidité
- Assurance Dentaire
il y a 8 jours
Senior Clinical Data Manager (Remote US or Canada)
Fortrea —À domicile
- De 80 000 $ à 145 000 $ par an
- Temps plein
- Télétravail
- Compétences rédactionnelles
- Anglais
- Baccalauréat
il y a 5 jours
Senior Clinical Trial Manager
Sitero LLC —Markham, ON
- Temps plein
- Travail hybride
- Baccalauréat
- Congés payés
Postuler rapidement
il y a 1 jour
Clinical Research Associate - Sponsor Dedicated - Bilingual
Syneos - Clinical and Corporate - Prod —À domicile
- Temps plein
- Télétravail
- Bilingue
- En présentiel
il y a 12 jours

Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : clinical trial manager (remote)

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Clinical Research Assistant

Everest Clinical Research -
Markham, ON

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Détails du poste

Permanent
De 45 000 $ à 70 000 $ par an

Profil recherché

Classement
Microsoft Office
Maîtrise
Baccalauréat
Sens de l'organisation
Compétences en informatique
Gestion des documents
Terminologie médicale
Compétences en communication

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 Research 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.

Key Accountabilities:

Receive medical writing and safety monitoring projects and project information from the Direct Manager or from the Work Mentor for the assigned projects. The project information may include the study protocol, Case Report Forms (CRFs), Investigator’s Brochure, etc.

Support medical writing and safety monitoring teams by performing QC review of document deliverables, including Clinical Study Reports (CSR), clinical study protocols, Informed Consent Forms, patient safety narratives, Safety Management Plans, scientific publications, and other documents intended for regulatory submissions.

Perform consistency review of document formats, styles, and overall layout according to a document style guide.

Perform data verification (QC) on statistical programming outputs against data source such as patient CRFs or other information provided. Report discrepancies found during the QC procedure.

Learn and perform document e-publishing for clinical trial and regulatory documents, including CSRs and tables, listings, and graphs (TLGs), which may include collection, scanning, electronic assembly, bookmarking, hyperlinking of documents, document cleaning, and header/pagination stamping, etc. Ensure the final product meets specific document publishing requirements and timelines.

May assist with hardcopy and electronic archiving of clinical trial documents, including filing within a Trial Master File, according to established document control and archiving practices.

May act as a DMC/DSMB Secretary, producing meeting minutes and assisting the DMC/DSMB Administrator to plan, organize, and coordinate meetings and serve as the primary contact for day‑to‑day operations between the members and the Sponsor.

Plan and manage deliverables and timelines in accordance with clinical trial project teams’ requirements.

Keep current on the training of Everest Guidance Documents and with the general requirements or guidelines issued by the pharmaceutical drug trial regulators and ICH.

Qualifications and Experience:

Bachelor degree in Clinical or Medical or Life Sciences with experience in the subject matter. M.Sc. or higher preferred.

Clinical trial experience in a pharmaceutical or Clinical Research Organization environment preferred.

Experience in Phase I through Phase IV clinical trials with knowledge of drug/medical device regulations and industry standards.

Experience with an accepted clinical data capture and management system preferred.

Strong verbal and written communication skills with the ability to understand and summarize medical terminology.

Good organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines.

Ability to maintain a high degree of confidentiality with clinical data and client’s proprietary data.

Detail-oriented, customer- and quality-focused.

Excellent interpersonal and teamwork skills.

Computing skills in Microsoft Office applications preferred.

Proven flexibility and adaptability when working in a team and independently, using good judgment in making decisions, preferred.

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: $45,000 - $70,000.

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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Je souhaite recevoir la dernière alerte emploi pour les postes de ce type : clinical trial manager (remote)

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