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Clinical Trial Assistant Jobs in Quebec

Senior Regional Clinical Trial Manager - Fully Remote Us Or Canada
By ICON Strategic Solutions At Canada
Responsible for Study Management and oversight of all Study Management functions internally and at the CROs
2+ years’ experience as a clinical Study, Trial or Project Manager.
Study Manager experience must be from Pharma, biotech or a CRO.
• Company value: (Senior Management, Culture & Values, Diversity & Inclusion)
Lead and manage the tactical execution of one or more clinical studies from study startup through database release.
Drive decision making and work closely with the Clinical Project Manager to provide input to operational strategy
Clinical Trial Coordinator Jobs
By Fortrea At Montreal, Quebec, Canada
Good organizational and time management skills
Manage sites to ensure subjects are complying with protocol requirements, study visits, and timelines.
Facilitate translation and back translation of all necessary documents as appropriate for local country requirements and as needed regionally.
Good communication skills, oral and written
Monitor site performance and implement action plans for sites not meeting expectations, in conjunction with the CRA.
Assist with the coordination of study visits and shipment of drug, ancillary supplies and laboratory kits/samples.
Clinical Assistant Jobs
By Vision Group At Boucherville, Quebec, Canada
You benefit from a free LASIK surgery, 3 weeks of vacation, 3 sick days, 1 floater & 1 wellness day.
You benefit from group insurance, telemedicine & RRSP match.
You have excellent communication skills, you speak English et français aussi. (Required)
A Look At Your Benefits
The selected candidate must be comfortable working out of both our LASIK MD Brossard and Boucherville clinics.*
You have a permanent full-time position. Monday to Friday 7AM-4PM (available to work early mornings and evenings when required).
Clinical Assistant Jobs
By LASIK MD At Gatineau, Quebec, Canada
You benefit from a free LASIK surgery, 3 weeks of vacation, 3 sick days, & 1 wellness day.
You benefit from group insurance, telemedicine & RRSP match.
You have excellent communication skills, you speak English et français aussi.
You have a permanent full-time position (32-40hrs/week).
You assist during the pre-op exams and fill the patient’s charts accurately.
You answer patient’s questions and ensure the best service.
Senior Local Trial Manager (Remote) (Canada) (Clinical)
By ICON Strategic Solutions At Canada
Advanced: 3 to 5+ years of trial management experience.
The efficient management of local vendors
Proactive risk management and budget forecasting
Timely review of trip reports submitted by Site Managers
A minimum of a 4-year Bachelor’s degree or relevant clinical experience is required
At least 2 years of Oncology experience required
Clinical Trial Assistant Jobs
By ICON Strategic Solutions At Canada
At least 2 years of related experience
Bachelor’s Degree preferred in scientific/medical discipline or equivalent experience.
Experience with clinical trials required
Experience with study start-up, maintanance, close-out of clinical studies
Demonstrated expertise and experience Clinical Trial Coordination
Ability to maintain Clinical Trial Tracking systems.
Clinical Trial Administrator Jobs
By Fortrea At Montreal, Quebec, Canada
Experience in the use of industry Clinical Trial Management Systems and Clinical Trial Master File Systems
Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support
Technologically proficient in MS office applications, Teams, SharePoint (file management and database)
Willing and able to support clinical operations team with report running, communications, and information management as needed
Perform other administrative duties as assigned by Line Manager, Project Managers or Clinical Trial Lead.
Minimum 1 year experience in clinical research or related work experience
Clinical Trial Coordinator Jobs
By Parexel At Canada
Effective time management, organizational and interpersonal skills, conflict management.
Clinical supply & non‐clinical supply management, in collaboration with other country roles.
Manage Labeling requirements and coordinate/sign translation change request.
Minimum 1-2 years in Clinical Research or relevant healthcare experience. Note - Specific experience requirements may vary depending on the Country
Maintenance of tracking tools. o Working knowledge of contract development, negotiation, approval, and maintenance (e.g., Clinical Trial Research Agreements (CTRAs)).
Completes training assigned by Client and/or EP, as necessary, including general training requirements, SOPs, and system and process related training.
Clinical Trial Coordinator - Regulatory - Montreal
By ICON Strategic Solutions At Montreal, Quebec, Canada
Completed job training (office management, administration, finance, health care preferred) or B.A./B.S. (Life Science preferred) or equivalent healthcare experience
Highly effective time management, organizational and interpersonal skills, conflict management
Clinical supply & non-clinical supply management, in collaboration with other country roles
Manage Labeling requirements and coordinate/sign translation change request
Excellent negotiation skills for CTCs in finance area
Minimum 1-2 yrs in Clinical Research or relevant healthcare experience
Clinical Trial Coordinator /Cta Montreal
By ICON Strategic Solutions At Canada
Clinical supply & non-clinical supply management, in collaboration with other country roles
Manage Labeling requirements and coordinate/sign translation change request
Regulatory & Site Start-Up responsibilities: Collaborate with other country roles to:
Track (e.g. essential documents) and report (e.g. Safety Reports)
Ensure collation and distribution of study tools and documents
Update clinical trial databases (CTMS) and trackers
Clinical Trial Assistant Jobs
By Montreal Health Innovations Coordinating Center (MHICC) At Montreal, Quebec, Canada

Hybride Anglais/Français requis Expérience en recherche clinique (TMF)

Clinical Trial Coordinator - R
By Parexel At Canada
Effective time management, organizational and interpersonal skills, conflict management.
Clinical supply & non‐clinical supply management, in collaboration with other country roles.
Manage Labeling requirements and coordinate/sign translation change request.
Minimum 1-2 years in Clinical Research or relevant healthcare experience. Note - Specific experience requirements may vary depending on the Country
Maintenance of tracking tools. o Working knowledge of contract development, negotiation, approval, and maintenance (e.g., Clinical Trial Research Agreements (CTRAs)).
Completes training assigned by Client and/or EP, as necessary, including general training requirements, SOPs, and system and process related training.
Clinical Trial Manager Jobs
By ICON plc At Montreal, Quebec, Canada
4 year degree or equivalent combination of education & experience
Prior monitoring experience is preferred
Demonstrated ability to drive the clinical deliverables of a study
Subject matter expertise in the designated therapeutic area
Ability to travel up to 20%
Clinical Trial Coordinator- Regulatory
By Labcorp At Québec, Quebec, Canada
Effective time management, organizational and interpersonal skills
B.A./B.S. (Life Science preferred) or equivalent healthcare experience
Minimum 1-2 years of clinical research or relevant healthcare experience
Fluent in French and English (verbal and written) and excellent communication skills
Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner
Update study documents when there are changes in study personnel/study amendments
Clinical Trial Coordinator Jobs
By LanceSoft, Inc. At Dorval, Quebec, Canada
Commercial or medical training (e.g., vocational qualification, bachelor’s degree), Medical records administrator or equivalent education, preferably with experience in clinical operations
•Supports preparation and translation of ICF into local languages (including vendor management if necessary)
Ideally several years of working experience with 1+ years´ of experience in clinical operations
•Ensures adherence to financial standards, prevailing legislation, ICH/GCP, IRB/IEC, Health Authority and SOP requirements
•Provides logistic support to SSU CRA, CRA, CPM, SSU Manager in all phases of the clinical trial
Understanding of clinical drug development with particular emphasis on trial setup, and contracting
Global Clinical Trial Associate (East Coast Hours)
By ICON Strategic Solutions At Canada
Typically requires 2 year of relevant work experience in the biopharmaceutical industry, or the equivalent combination of education and experience.
Basic working knowledge of GCP, CFR and ICH guidelines and clinical trial operations
Written, verbal and interpersonal skills to exchange straightforward information
Organizes Study Team meetings and prepares meeting minutes
Assists with organizing Investigator Meetings
Assists with preparation and review of study documents
Office Assistant C (Clinical Projects Assistant)-2
By McGill University At Montreal, Quebec, Canada
Organiser, classer et archiver des documents.
Saisir des informations dans des logiciels de saisie électronique de données et des feuilles de calcul.
Guider les patients lors de leur visite au Neuro
Transporter les échantillons du point de collecte jusqu'à l'équipe de traitement du laboratoire.
Identifier les informations pertinentes dans les dossiers papier ou électroniques à la demande des coordinateurs de recherche
Comment postuler à un emploi (pour les candidats externes)
Clinical Administrative Assistant Jobs
By AvantSleep At Moncton, New Brunswick, Canada
Strong client service skills (our patients deserve the best).
A professional and mature demeanor, with strong communication skills.
Very strong organizational and multitasking skills.
Experience using an EMR system is an asset.
Ready and willing to learn and upgrade your skills.
Experience in health care or sleep therapy is an asset but not required. Training is provided.

Are you looking for a rewarding career in clinical research? We are looking for a Clinical Trial Assistant to join our team and help us make a difference in the lives of patients. As a Clinical Trial Assistant, you will be responsible for coordinating and managing clinical trial activities, ensuring compliance with regulatory requirements, and providing administrative support. If you are passionate about clinical research and have excellent organizational and communication skills, this could be the perfect job for you!

Overview A Clinical Trial Assistant (CTA) is a professional who assists in the management of clinical trials. The CTA is responsible for providing administrative and operational support to the clinical trial team. This includes tasks such as data entry, tracking and filing documents, and coordinating with other departments. Detailed Job Description A Clinical Trial Assistant is responsible for providing administrative and operational support to the clinical trial team. This includes tasks such as data entry, tracking and filing documents, scheduling meetings, and coordinating with other departments. The CTA is also responsible for ensuring that all clinical trial documents are accurate and up-to-date. The CTA may also be responsible for preparing reports, tracking progress, and providing feedback to the clinical trial team. Job Skills Required
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office Suite
• Knowledge of clinical trial processes and regulations
• Attention to detail
• Ability to multitask
• Ability to work under pressure
Job Qualifications
• Bachelor’s degree in a related field
• Previous experience in clinical trials or research
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
Job Knowledge
• Knowledge of clinical trial processes and regulations
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of data management systems
Job Experience
• Previous experience in clinical trials or research
• Experience in data entry and data management
• Experience in preparing reports and tracking progress
Job Responsibilities
• Data entry and data management
• Tracking and filing documents
• Scheduling meetings
• Coordinating with other departments
• Preparing reports and tracking progress
• Ensuring accuracy and up-to-date clinical trial documents
• Providing feedback to the clinical trial team