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

FSP Clinical Research Associate I - Ontario Canada
Thermo Fisher Scientific —Toronto, ON
- De 62 000 $ à 107 477 $ par an
- Temps plein
- Soins infirmiers
- Anglais
- Microsoft Office
il y a 2 jours
Research Assistant (SRI) - Evaluative Clinical Sciences - Casual 2026-18011
Sunnybrook Health Sciences Centre —Toronto, ON
- Baccalauréat
- Saisie de données
- Sens de l'organisation
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Lead Clinical Research Associate
PSI CRO —Toronto, ON
- De 124 000 $ à 153 000 $ par an
- Temps plein
- Télétravail
- Anglais
- Microsoft Office
- Baccalauréat
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Senior Clinical Research Associate
PSI CRO —Toronto, ON
- De 120 000 $ à 150 000 $ par an
- Temps plein
- Télétravail
- Anglais
- Microsoft Office
- Baccalauréat
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Research Associate
Humber River Health —Greater Toronto Area, ON
- De 49,91 $ à 62,43 $ de l’heure
- Temporaire
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
il y a 2 jours
ASSOCIATE SCIENTIST I - AGS
DiaSorin —Toronto, ON
- De 55 000 $ à 65 000 $ par an
- Temporaire
- Microsoft Powerpoint
- Microsoft Word
- Expérience en laboratoire
il y a 10 jours
Experienced Clinical Research Associate (CRA II/Sr CRA) - Toronto, Ontario Canada
Thermo Fisher Scientific —Toronto, ON
- De 75 000 $ à 125 000 $ par an
- Temps plein
- Soins infirmiers
- Anglais
- Microsoft Office
il y a 9 jours
QA Associate - Eurofins BioPharma Product Testing Toronto, Inc.
Eurofins Canada BioPharma —Toronto, ON
- 52 000 $ par an
- Embauche urgente
- Travail hybride
- Contrôle de l'inventaire
- Compétences informatiques
- Expérience en laboratoire
- Jours fériés payés
- Assurance Invalidité
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Administrative Coordinator
University of Toronto —Toronto, ON
- De 67 916 $ à 86 855 $ par an
- Temps plein
- Microsoft Outlook
- Expérience administrative
- SharePoint
il y a 2 jours
Associate Director, Project Management
Everest Clinical Research-Can —Markham, ON
- De 170 000 $ à 220 000 $ par an
- Télétravail
- Maîtrise
- Capacités de présentation
- Baccalauréat
- Assurance Invalidité
- Assurance Dentaire
Postuler rapidement
il y a 11 jours
Administrative Assistant (SRI) - Evaluative Clinical Sciences - Regular Full-time 2026-17356
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Microsoft Outlook
- Expérience administrative
- Baccalauréat
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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
- Mentorat
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Research Associate (SRI) - Physical Sciences - Regular Full-time 2025-15843
Sunnybrook Health Sciences Centre —Toronto, ON
- Temps plein
- Doctorat
- Anglais
- Sens de l'organisation
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Director, Project Management
Everest Clinical Research-Can —Markham, ON
- De 190 000 $ à 240 000 $ par an
- Télétravail
- Maîtrise
- Capacités de présentation
- Baccalauréat
- Assurance Invalidité
- Assurance Dentaire
Postuler rapidement
il y a 12 jours
Chef de projet associé, Mesure (Measurement Associate Project Manager), IQVIA Digital
IQVIA —Toronto, ON
- De 70 500 $ à 117 500 $ par an
- Temps plein
- Service à la clientèle
- Baccalauréat
- Compétences en informatique
Post-Doctoral Fellow (SRI) - Sunnybrook Research Institute - Temporary Full-Time 2026-18500
Sunnybrook Health Sciences Centre —Toronto, ON
- Temporaire
- Doctorat
- Compétences rédactionnelles
- Recherche
- Mesures de protection COVID-19
Postuler rapidement
il y a 12 jours

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FSP Clinical Research Associate I - Ontario Canada
Thermo Fisher Scientific —Toronto, ON
Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
De 62 000 $ à 107 477 $ par an
il y a 2 jours
Research Assistant (SRI) - Evaluative Clinical Sciences - Casual 2026-18011
Sunnybrook Health Sciences Centre —Toronto, ON
Bachelor’s degree in Health Sciences or related discipline. Minimum 1 year of relevant work experience. Abstracting data from SunnyCare (EPR) related to head…
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FSP Clinical Research Associate I - Ontario Canada

Thermo Fisher Scientific -
Toronto, ON

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Détails du poste

Temps plein
De 62 000 $ à 107 477 $ par an
Il y a 2 jours

Profil recherché

Soins infirmiers
Analyse des causes fondamentales des défauts
Recherche clinique
Amélioration des processus
Actions correctives et préventives (CAPA)
Anglais
Microsoft Office
Baccalauréat
Conduite de véhicule
Rédaction de rapports
Orientation axée sur le service à la clientèle
Analyse des causes profondes
Procédures opératoires normalisées (PON)
Terminologie médicale
Compétences en communication
Interaction avec les clients
Coordination d'équipe
Suivi de l'avancement des projets
Permis de conduire
Gestion du temps

Description complète du poste

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Research Associate I – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to perform and coordinate different aspects of the clinical monitoring and site management process. As a Clinical Research Associate I, you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings
resolution. Investigates and follows-up on findings as applicable.
Participates in investigator meetings as necessary. May help to identify potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials.
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
Provides trial status tracking and progress update reports to the team as required. Ensures study systems are complete, accurate and updated per agreed study conventions (e.g. Clinical Trial Management System).
Facilitates effective communication between investigative sites, the client company and internal project teams through written, oral and/or electronic contacts. Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains and completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to the project team by assisting in preparation of project publications/tools and sharing ideas/suggestions with team members. Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Minimal clinical monitoring experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 years) in a clinical environment where experience is gained in clinical trials, medical terminology, medical research, clinical research or health care or experience in a health sciences field with formal training in medical terminology and anatomy may be considered.
Valid driver's license where applicable.

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Basic medical/therapeutic area knowledge and understanding of medical terminology
Ability to attain and maintain a working knowledge of ICH GCPs and applicable regulations and procedural documents
Good oral and written communication skills, with the ability to communicate effectively with medical personnel
Good interpersonal skills
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues
Good organizational and time management skills
Ability to remain flexibile and adaptable in a wide range of scenarios
Well-developed critical thinking skills, including but not limited to: critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
Ability to manage Risk Based Monitoring concepts and processes
Ability to work in a team or independently as required
Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
Good English language and grammar skills

Working Conditions and Environment:

Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals. May also include extended overnight stays.
Exposure to biological fluids with potential exposure to infectious organisms.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions.

Compensation

The estimated annualized pay range for this position in Ontario is $62,000.00–$107,477.00.

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clinical research associate emplois - markham, on

FSP Clinical Research Associate I - Ontario Canada

Research Assistant (SRI) - Evaluative Clinical Sciences - Casual 2026-18011

Lead Clinical Research Associate

Senior Clinical Research Associate

Research Associate

ASSOCIATE SCIENTIST I - AGS

Experienced Clinical Research Associate (CRA II/Sr CRA) - Toronto, Ontario Canada

QA Associate - Eurofins BioPharma Product Testing Toronto, Inc.

Administrative Coordinator

Associate Director, Project Management

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

Sr. Clinical Operations Lead (Clinical Trial Manager)

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

Director, Project Management

Chef de projet associé, Mesure (Measurement Associate Project Manager), IQVIA Digital

Post-Doctoral Fellow (SRI) - Sunnybrook Research Institute - Temporary Full-Time 2026-18500

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