20 meilleures offres (clinical research coordinator, 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
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 Research Associate - Canada
Syneos - Clinical and Corporate - Prod —À domicile
- Temps plein
- Télétravail
- Capacités de présentation
- Baccalauréat
- Déplacements à prévoir
Bilingual Sr. Clinical Research Associate
Alimentiv —Toronto, ON
- De 78 000 $ à 130 000 $ par an
- Temps plein
- Télétravail
- Bilingue
- Anglais
- Déplacements à prévoir
Postuler rapidement
Clinical Data Coordinator
Alimentiv —London, ON
- De 41 000 $ à 68 000 $ par an
- Temps plein
- Télétravail
- Compétences en communication
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
Clinical Research Associate - Sponsor Dedicated - Bilingual
Syneos - Clinical and Corporate - Prod —À domicile
- Temps plein
- Télétravail
- Bilingue
- En présentiel
il y a 12 jours
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
Bilingual, Freelance / Contractual Clinical Research Associate, Montreal,
Indero —À domicile
- Télétravail
- Microsoft Powerpoint
- Bilingue
- Microsoft Word
Postuler rapidement
11 h
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
Postuler rapidement
11 h
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
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
Intake Coordinator/Counsellor
Intersect Youth and Family Services —Prince George, BC
- De 33,69 $ à 42,45 $ de l’heure
- Temps plein
- Maîtrise
- Psychologie
- Sens de l'organisation
- Indemnité de déménagement
- Assurance Dentaire
Postuler rapidement
11 h
Infirmière Praticienne Spécialisée en Santé Mentale (IPSSM) -Nurse Practitioner
Field Trip Health —Province de Québec
- 150 $ de l’heure
- Temps partiel
- Télétravail
- Administration de médicaments
- Maîtrise
- Soins médicaux
- Heures d'arrivée et de départ flexibles
Postuler rapidement
Virtual Care Nurse Practicioner
Cleveland Clinic Canada —Saskatchewan
- À partir de 80 $ de l’heure
- 12 Heures
- Télétravail
- Travail à domicile
- Heures d'arrivée et de départ flexibles
Postuler rapidement
il y a 5 jours
Clinical Trial Coordinator- Finance- FSP
Parexel —À domicile
- Télétravail
- Microsoft Excel
- Anglais
- Microsoft Office
il y a 12 jours
Senior Clinical Research Associate
Parexel —À domicile
- Télétravail
- Baccalauréat
- Déplacements à prévoir
- Compétences en informatique
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
Senior Clinical Trial IWRS Monitor
Everest Clinical Research —Markham, ON
- De 70 000 $ à 90 000 $ par an
- Télétravail
- Informatique
- Service à la clientèle
- Gestion de projet
- Assurance Invalidité
- Assurance Dentaire
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

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

En vous connectant à votre compte, vous acceptez les conditions d'utilisation, la politique relative aux fichiers témoins et la politique de confidentialité de SimplyHired.

Découvrir les offres d'emploi dans d'autres lieux

clinical research coordinator jobs near remote

Clinical Lead Nurse (London, ON) : offres d'emploi

Clinical Research Associate (Remote) : offres d'emploi

Clinical Project Manager (Remote) : offres d'emploi

Clinical Research Associate (Markham, ON) : offres d'emploi

Clinical Assistant (Markham, ON) : offres d'emploi

Nurse Practitioner (Quebec Province) : offres d'emploi

Clinical Research Associate (Montréal, QC) : offres d'emploi

Nurse (Saskatchewan) : offres d'emploi

Clinical Trial Manager (Remote) : offres d'emploi

Senior Clinical Research Associate (Ontario) : offres d'emploi

Mental Health Nurse (Ontario) : offres d'emploi

Clinical Lead Nurse (Penticton, BC) : offres d'emploi

Clinical Lead Nurse (Vancouver, BC) : offres d'emploi

Clinical Assistant (Kingston, ON) : offres d'emploi

Clinical Lead Nurse (Stouffville, ON) : offres d'emploi

Clinical Research Remote (Vancouver, BC) : offres d'emploi

Clinical Research Associate (East York, ON) : offres d'emploi

Research Assistant (Ottawa, ON) : offres d'emploi

Non Clinical Physiotherapy (Ontario) : offres d'emploi

Clinical Research Associate (Edmonton, AB) : offres d'emploi

Clinical Trial Assistant I

Everest Clinical Research -
Markham, ON

Postuler rapidement

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.

Postuler rapidement

Affinez votre recherche

clinical research coordinator emplois - remote

Clinical Trial Assistant I

Lead Clinical Research Associate

Clinical Research Associate - Canada

Bilingual Sr. Clinical Research Associate

Clinical Data Coordinator

Clinical Trial Associate 2

Clinical Research Associate - Sponsor Dedicated - Bilingual

Clinical Trial IWRS Monitor (Overnight)

Bilingual, Freelance / Contractual Clinical Research Associate, Montreal,

Clinical Trial Manager II / Gestionnaire d’essais cliniques II, Canada, remote

Clinical Project Manager

Bilingual Clinical Research Associate (CRA) - Montreal

Intake Coordinator/Counsellor

Infirmière Praticienne Spécialisée en Santé Mentale (IPSSM) -Nurse Practitioner

Virtual Care Nurse Practicioner

Clinical Trial Coordinator- Finance- FSP

Senior Clinical Research Associate

Sr. Clinical Operations Lead (Clinical Trial Manager)

Senior Clinical Trial IWRS Monitor

Gestionnaire d'essais cliniques II, IQVIA Biotech/Clinical Trial Manager II, IQVIA Biotech

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

Related Searches

Découvrir les offres d'emploi dans d'autres lieux

Outils pour les chercheurs d'emploi

Outils Employeurs

Parcourir

Garder le contact