Montréal, Qc Clinical data Jobs – 194 Openings This Week

Clinical Trial Coordinator – Regulatory & Finance - Hybrid, Montreal
Fortrea —Montréal, QC
- Full-time
- Hybrid work
- Bilingual
- English
- Bachelor's
Lead Clinical Research Associate
Altasciences —Montréal, QC
- $82,000–$136,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Designated paid holidays
- Dental care
14d
Research Assistant
Centre universitaire de santé McGill - Institut de Recherche —Montréal, QC
- Temporary
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Designated paid holidays
- Employee assistance program
Quick apply
Full-time Clinical Research Assistant
Lady Davis Institute for Medical Research/Jewish General Hospital —Montréal, QC
- 8 hour shift
- Bilingual
- Writing skills
- English
- Disability insurance
- Dental care
9d
Manager, Clinical Data Management
Alimentiv —Montréal, QC
- $99,500–$160,000 a year
- Full-time
- Remote
- Leadership
- Dental care
- Tuition reimbursement
Quick apply
6d
Epic Non-Clinical Associate Manager or Manager
Accenture —Montréal, QC
- $82,600–$132,600 a year
- Full-time
- Hybrid work
- Microsoft Excel
- English
- Bachelor's
Clinical Research Coordinator
McGill University —Montréal, QC
- $33.05–$40.97 an hour
- Full-time
- Hybrid work
- Nursing
- English
- Bachelor's
- Dental care
- Paid time off
Clinic Administrator
McGill University —Montréal, QC
- $33.05–$40.97 an hour
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Bilingual
- Microsoft Word
- Dental care
- Paid time off
6d
Research Assistant 2
McGill University —Montréal, QC
- $31.44 an hour
- Full-time
- English
- Master's degree
- Communication skills
Clinical Research Coordinator
Centre universitaire de santé McGill - Institut de Recherche —Montréal, QC
- Temporary
- Nursing
- English
- Bachelor's
- Paid sick leave
Quick apply
Research Assistant
Centre universitaire de santé McGill - Institut de Recherche —Montréal, QC
- Temporary
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Designated paid holidays
- Employee assistance program
Quick apply
6d
Clinical Trial Manager II
Syneos - Clinical and Corporate - Prod —Montréal, QC
- Full-time
- Presentation skills
- Bachelor's
- Travel
Research Assistant
Centre universitaire de santé McGill - Institut de Recherche —Montréal, QC
- Temporary
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Spanish
- Designated paid holidays
- Employee assistance program
Quick apply
Epic Clinical Associate Manager or Manager
Accenture —Montréal, QC
- $82,600–$132,600 a year
- Full-time
- Hybrid work
- Microsoft Excel
- English
- Bachelor's
Clinical Quality Control Associate II
Altasciences —Montréal, QC
- Full-time
- Bilingual
- English
- Microsoft Office
- Dental care
- Employee assistance program
Data Manager
McGill University —Montréal, QC
- $73,470–$110,210 a year
- Full-time
- Hybrid work
- Bilingual
- English
- Research
- Dental care
- Paid time off
Ultrasound Technologist
TELUS —Montréal, QC
- $70,000–$130,000 a year
- Part-time
- Bilingual
- English
- Analysis skills
Medical Imaging Technologist (Mammography certification)
TELUS —Montréal, QC
- $29–$53 an hour
- Full-time
- Bilingual
- English
- Computer skills
Screening Quality Control Associate
Altasciences —Montréal, QC
- Overtime
- Bilingual
- Customer service
- English
- Designated paid holidays
- Dental care
12d
Manager, Clinical Quality Control Department
Altasciences —Montréal, QC
- Full-time
- Hybrid work
- Bilingual
- English
- Microsoft Office
- Dental care
- Paid time off
Administrative Student Affairs Coordinator
McGill University —Montréal, QC
- $31.19–$38.65 an hour
- Full-time
- Bilingual
- English
- Databases
7d
Clinical Research Manager
Centre universitaire de santé McGill - Institut de Recherche —Montréal, QC
- $71,598.80–$132,969.20 a year
- Temporary
- Bilingual
- Doctoral degree
- English
- Designated paid holidays
- Employee assistance program
Quick apply
Bilingual Senior Program Manager - Nurse Practitioner Team Lead
TELUS —Montréal, QC
- $86,000–$136,000 a year
- Temporary
- Remote
- Bilingual
- Google Suite
- Data analysis skills
14d
Procurement Specialist (Medical Equipment & Supplies)
Wealthy Group of Companies LLC —Lasalle, QC
- $75,000–$85,000 a year
- Full-time
- Microsoft Excel
- Inventory management
- ERP systems
Quick apply
5d
Nurse Case Manager
Bayshore HealthCare —Montréal, QC
- Full-time
- Bilingual
- Nursing
- Microsoft Excel

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Clinical Trial Coordinator – Regulatory & Finance - Hybrid, Montreal

Fortrea
Montréal, QC

Apply Now

Job details

Full-time

Skills

Bilingual
French
SAP
English
Bachelor's
Organizational skills
Computer skills
Communication skills
Time management

Full job description

Fortrea's FSP team is hiring a Clinical Trial Coordinator- Regulatory - Hybrid in Montreal, Canada. Must be bilingual in French & English. Candidates with strong organizational skills, attention to details, and the ability to manage financial processes effectively will be particularly well suited for the role.

Job Overview:

We are seeking a Clinical Trial Coordinator – Regulatory to serve as contact for project team and investigative sites, conduct site contacts and document contacts for assigned sites as required per study guidelines, including creating contact reports for each telephone session (outbound or inbound) with sites.

Responsibilities:

Serve as contact for project team and investigative sites, conduct site contacts and document contacts for assigned sites as required per study guidelines, including creating contact reports for each telephone session (outbound or inbound) with sites.

Monitor site performance and implement action plans for sites not meeting expectations, in conjunction with the CRA.

Assist CRAs with preparation for site visits ( i.e. running reports, QC of files (checking for missing documents), resolving action items from previous visits).

Perform Case Report Form review, query generation and resolution against established data review guidelines, under direct supervision on Fortrea or client data management systems, as assigned by management.

Assist with the coordination of study visits and shipment of drug, ancillary supplies and laboratory kits/samples.

Manage sites to ensure subjects are complying with protocol requirements, study visits, and timelines.

Liaise with the project team and others to distribute and track clinical trial supplies, e.g. Case Report Forms, study medication, lab kits, ensuring that sites have sufficient supplies to continue recruitment.

Proactively work with sites and project teams to ensure maintenance activities (including Amendments, revised documents, etc.) are completed for assigned sites as applicable in region.

Demonstrate an understanding of the purpose of CTMS, how to use it, and how to navigate within the different sections. To enter weekly details in CTMS or as per study requirement.

Assist in submissions and notifications to Ethics Committees and Regulatory Authorities as applicable in region .

Facilitate translation and back translation of all necessary documents as appropriate for local country requirements and as needed regionally.
Attend , as needed, meetings (investigator, sponsor, kick-off, face-to-face) and to present at the meetings.

Processing site invoices in a timely and accurate manner
Managing routine site payments and reimbursements
Ensuring payment related activities are completed in accordance with study and financial requirements
Collaborating with internal stakeholders to resolve payment inquiries and discrepancies as needed
R equired to work within SUVODA and COMET/SAP

Requirements:

At least one year of experience in a related field, ( e.g. medical, clinical, pharmaceutical, laboratory research, data analysis, data management or technical writing).

1-2 years of clinical research is required .

Basic understanding of biology and biological processes

Ability to monitor study sites according to protocol monitoring guidelines, SOPs, ICH Guidelines and GCP.

Good organizational and time management skills

Good communication skills, oral and written

Exhibit s general computer literacy

Works efficiently and effectively in a matrix environment

Qualifications (Minimum Required):

University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology).
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

This position is performed through a combination of remote work and in-person at the client's Head Office (2-3 times/week).

Physical Demands/Work Environment:

General Office Environment.

Learn more about our EEO & Accommodations request here .

Apply Now

Refine Your Search

clinical data jobs in montréal, qc

Clinical Trial Coordinator – Regulatory & Finance - Hybrid, Montreal

Lead Clinical Research Associate

Research Assistant

Full-time Clinical Research Assistant

Manager, Clinical Data Management

Epic Non-Clinical Associate Manager or Manager

Clinical Research Coordinator

Clinic Administrator

Research Assistant 2

Clinical Research Coordinator

Research Assistant

Clinical Trial Manager II

Research Assistant

Epic Clinical Associate Manager or Manager

Clinical Quality Control Associate II

Data Manager

Ultrasound Technologist

Medical Imaging Technologist (Mammography certification)

Screening Quality Control Associate

Manager, Clinical Quality Control Department

Administrative Student Affairs Coordinator

Clinical Research Manager

Bilingual Senior Program Manager - Nurse Practitioner Team Lead

Procurement Specialist (Medical Equipment & Supplies)

Nurse Case Manager

I want to receive the latest job alerts for clinical data in montréal, qc

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