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Clinical Trial Assistant Jobs

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.
Clinical Trial Research Nurse
By The University of British Columbia At Hospital, British Columbia, Canada
Demonstrates a commitment to enhancing one’s own awareness, knowledge, and skills related to equity, diversity, and inclusion
Registered Nurse with BCCNP plus a minimum of one year of nursing experience.
Attentive to detail, with the ability to work quickly and accurately. Superior organizational skills.
Strong analytical, problem solving and decision-making skills.
This offer is conditional upon successful completion of a Criminal Record Check.
Obtain informed consent for study participants.
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 Operations Specialist
By System One At Toronto, Ontario, Canada
Planning, coordination and conduct of complex, regulatorily defined tasks
Seamless trial operation and communication to all applicable stakeholders
Timely delivery of all the materials, documentation and information needed to setup, execute, and delivery of the assigned trial(s)
Overnight of trial supplies, documentation, submissions, and other operational parameters
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 Contracts Administrator
By Amgen At Mississauga, Ontario, Canada
1+ years experience in contracting, finance administration, project management, or other experience in life sciences or medical field
Advances contract and budget issues to Legal, Pricing Group, and/or Regional Clinical Trial Manager as appropriate.
Configures site contracts and study specific requirements into eClinical payment portal.
Manages internal collaborator needs and expectations through regular communication regarding progress and status of pending contract and payment requests.
Work experience in clinical research acquired while working on clinical trials for a biotech/pharma company or CRO
Prior experience or robust understanding of clinical site contracting and payment processes
Clinical Trial Coordinator Jobs
By Source Nutraceutical, Inc. At Winnipeg, Manitoba, Canada
Knowledge and/or experience in working with Clinical Trial Management System (CTMS), e-consent processes, e-data collection (EDC), and storage.
Experience working with project management software.
Knowledge and experience in ICH/GCP and Good Documentation Practice (GDP).
Additional education and/or professional certifications would be an asset, including:
Certified Associate of Project Management (CAPM).
The ability to analyze, organize, prioritize, and manage multiple projects.
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 Assistant Jobs
By Halton Multicultural Council Inc At Brampton, Ontario, Canada
- Implement effective management plans that include preventive and therapeutic interventions
-INTERNATIONAL MEDICAL GRADUATE with an experience in independent practice
Under the supervision of the licensed physician, Clinical Assistant will perform the following tasks:
- Appropriately adapt their scope of practice within the specific clinical setting of the supervising physician
- Perform a focused physical examination that is relevant and accurate
- Fully document all aspects of patient care and assist with the completion of all required documentation
Clinical Operations Assistant Jobs
By Prenuvo At Vancouver, British Columbia, Canada
Excellent organizational skills with the ability to multitask and prioritize responsibilities effectively
We offer a comprehensive benefits package including health, dental, vision, including Mental Health coverage, to support you and your family
Assist in the day to day requirements of releasing medical reports, scheduling NP calls, and other tasks as required
Proven experience in a healthcare setting, preferably in a clinical or hospital environment
Strong interpersonal and communication skills to interact with patients, healthcare professionals, and other staff members
Knowledge of medical ethics, confidentiality regulations, and infection control protocols
Clinical Administrative Assistant Jobs
By AvantSleep At Fredericton, New Brunswick, Canada
Experience working in a management or supervisory role is considered an asset.
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.
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%

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