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Added 1 hour ago
GE
Stage Bar Server
Grey Eagle Resort & Casino
Calgary, AB
- Full-time
Report to work on time, prepared for the scheduled shift, and in full compliance with established uniform, grooming, hygiene, and appearance standards.
Added 1 hour ago
GE
Reservation Agent - Internal Candidates Only
Grey Eagle Resort & Casino
Calgary, AB
- Full-time
Under the direction of the Front Office supervisor, Assistant Front Office Manager, and/or Front Office Manager, the Reservation Agent promotes and sells room nights to existing and…
Added 1 hour ago
GE
Blaze Bar & Grill Server
Grey Eagle Resort & Casino
Calgary, AB
- Full-time
Report to work on time, prepared for the scheduled shift, and in full compliance with established uniform, grooming, hygiene, and appearance standards.
Added 2 hours ago
F
School Supervisor
Fitzrovia
Toronto, ON
- $75,000 to $85,000 CAD / year
- Full-time
As we are a highly collaborative team, the successful candidate will be required to work on-site full-time.
Added 4 hours ago
C
General Labor
Cascades
Toronto, ON · Scarborough, ON
- Full-time
Full-time position with guaranteed hours for job stability
Added 5 hours ago
RL
Sr. CNC Manufacturing Specialist (6 months contract)
Romet Limited
ON · Mississauga, ON
- Full-time
Opportunties for permanent and full-time positions
Added 6 hours ago
R|
Clinical Research Nurse - Occasional Pool
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
…care, ICU, and/or infusion therapy. These nurses will support full-time CIM nursing staff by assisting with clinical trial-related activities, particularly those occurring outside of…
Added 6 hours ago
R|
Receiving, Distribution and Package Delivery Clerk
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Position summary Reporting to the Receiving and Distribution Supervisor, the incumbent is responsible for receiving, verifying, sorting, temporarily storing, internally distributing and…
Added 6 hours ago
R|
Clinical Research Coordinator - Regulatory Affairs (CIM)
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Status : Temporary full-time (6 months replacement)
Added 6 hours ago
R|
Clinical Research Coordinator
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Status: Temporary, full time (35-hour workweek)
Added 6 hours ago
R|
Clinical Trial Financial Control Analyst, Oncology Portfolio
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Status : Temporary -Full-time (35 hours work week) - 12 months contract
Added 6 hours ago
R|
Clinical Research Manager
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Added 6 hours ago
R|
Fellowship and Bursary Administrative Assistant
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
…and other bursary-funded streams. The incumbent manages the full trainee life cycle: selection and funding preparation, payroll and HR onboarding, status tracking, and budget and tuition…
Added 6 hours ago
R|
Clinical Research Coordinator – Nurse - CIM - Phase 1 Oncology
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Status : Temporary Full-time, maternity leave replacement.
Added 6 hours ago
R|
Clinical Research Coordinator - Nurse
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Status: Temporary, full time (35-hour workweek)
Added 6 hours ago
R|
Research Assistant - Public Engagement
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
Under the direction of the immediate supervisor, the incumbent will:
Added 6 hours ago
R|
Clinical Research Coordinator - Nurse (CIM)
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Contract
Status : Temporary full time (35 hours/weeks - 12-month contract)
Added 7 hours ago
PF
Delivery Driver
Performance Food Group
Ottawa, ON
- Full-time
…Scholarship Opportunities for children of associates, Paid Time Off, and much…
Added 8 hours ago
T&
Production Supervisor
Tallow & Fries, Inc.
Mississauga, ON
- Full-time
We are seeking dedicated and experienced results-driven Shift Supervisor to lead and oversee all operations on our automated frozen french fries production line during an assigned shift in…
Added 10 hours ago
SG
Materials Supervisor
S3 Group Ltd.
Swift Current, SK
- Full-time
Added 12 hours ago
TG
Welder 210/220
Trench Group
Toronto, ON · Scarborough, ON
- Full-time
Scarborough, ON | Union | Full-Time | Mid-Level (3+ years)
Added 12 hours ago
SP
Clinical Supervisor, Part-Time (Nurse RN/RPN Preferred) - Part-Time (Travel Required)
Seneca Polytechnic
King City, ON
- Part-time
Seneca is Canada’s leading, and Ontario's first, polytechnic with more than 40,000 full-time students and 18,500 part-time students. Since opening our doors for the first time more than 55…
Added 13 hours ago
GE
Stage Bar Server
Grey Eagle Resort & Casino
Calgary, AB
- Full-time
Report to work on time, prepared for the scheduled shift, and in full compliance with established uniform, grooming, hygiene, and appearance standards.
Added 13 hours ago
GE
Blaze Bar & Grill Server
Grey Eagle Resort & Casino
Calgary, AB
- Full-time
Report to work on time, prepared for the scheduled shift, and in full compliance with established uniform, grooming, hygiene, and appearance standards.
Added 14 hours ago
AG
Warehouse Technician (General)
Avmax Group
Calgary, AB
- Full-time
The Warehouse Technician (General) reports directly to the Shipping Supervisor.

Tata Consultancy Services

Document Publisher CMC

Toronto, ON, Canada

$90,000 to $110,000 CAD / year · Full-time

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Job details

Pay: $90,000 to $110,000 CAD / year
Job type: Full-time
Apply by: Dec 4, 2026
Posting language: English
Posted: Nov 4, 2026

Original job description

Inclusion without Exception

Tata Consultancy Services (TCS) is an equal opportunity employer, and embraces diversity in race, nationality, ethnicity, gender, age, physical ability, neurodiversity, and sexual orientation, to create a workforce that reflects the societies we operate in. Our continued commitment to Culture and Diversity is reflected in our people stories across our workforce and implemented through equitable workplace policies and processes.

TCS has been serving the Canadian marketplace for more than 35 years and today is the technology partner of choice for many of the country's leading organizations. As one of the largest IT services providers in Canada and globally, TCS is aiming to become the world's largest AI-led technology services company and is enabling its clients to transform themselves across the full AI stack, from infrastructure to intelligence.

Rooted in the heritage and values of the Tata Group, TCS is focused on creating long-term value for its clients, investors, employees, and the communities it serves. With a highly skilled workforce supporting customers from coast to coast, TCS has consistently been recognized as a Top Employer by the Top Employers Institute, including a recent top ranking at the country level.

TCS also sponsors 14 of the world's most prestigious marathons and endurance events, including the TCS Toronto Waterfront Marathon, reflecting its commitment to health, sustainability, and community empowerment.

eCRF Document Specialist (Document Publisher CMC)

Educational Qualification

Bachelor’s degree in Life Sciences, Pharmacy, or a related discipline
Master’s degree is preferred

Role Summary

The eCRF Document Specialist will support electronic case report form documentation and electronic submission readiness activities. The role involves formatting, standardizing, optimizing, reviewing, and performing quality checks on clinical trial documents according to established standards and timelines.

Key Responsibilities

Perform electronic submission readiness activities for different types of eCRF documentation, including:
Subject CRF
Annotated CRF (aCRF)
Sample CRF
Define documents
Clinical Study Data Reviewer’s Guide (cSDRG/SDRG)
Standardize document and file names according to established naming conventions.
Create and maintain the required folder structures for clinical trial documentation.
Format documents according to applicable standards and submission requirements.
Optimize documents and perform quality control checks within established timelines.
Review completed documents using the designated document-review tool to ensure accuracy, consistency, and high-quality deliverables.
Identify and resolve issues during the document review process.
Consolidate queries or issues identified while processing files for specific clinical trials.
Communicate queries to the appropriate points of contact and provide potential solutions for consideration and formal approval.
Ensure all assigned documents are completed accurately and delivered within the agreed timelines.
Perform additional responsibilities or activities assigned by the supervisor.

Required Skills

Basic understanding of clinical trial documentation and eCRF processes
Knowledge of CRF, aCRF, Define, cSDRG, and SDRG documents
Strong document formatting and publishing skills
Good attention to detail and quality
Ability to follow naming conventions, templates, and document standards
Strong organizational and time-management skills
Ability to identify, document, and communicate processing issues
Good written and verbal communication skills
Ability to work independently and collaboratively within a team

Preferred Skills

Exposure to clinical document publishing or electronic submission readiness
Familiarity with clinical research or pharmaceutical documentation
Experience with document optimization and quality-control processes
Familiarity with automated document-review tools

Salary Range - CA$ 90,000 - CA$ 110,000 Per Year

Tata Consultancy Services Canada Inc. is committed to meeting the accessibility needs of all individuals in accordance with the Accessibility for Ontarians with Disabilities Act (AODA) and the Ontario Human Rights Code (OHRC). Should you require accommodation during the recruitment and selection process, please inform Human Resources.

Thank you for your interest in TCS. Candidates that meet the qualifications for this position will be contacted within a 2-week period. We invite you to continue to apply for other opportunities that match your profile.

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More about this job

Responsibilities

Prepare, format, standardize, optimize, and quality-check eCRF and related clinical trial documents for electronic submission readiness. Review documents for accuracy and consistency, resolve or communicate processing issues, and deliver assigned work within agreed timelines.

Requirements

A bachelor’s degree in life sciences, pharmacy, or a related discipline is required, while a master’s degree is preferred. Candidates should understand clinical trial documentation and eCRF processes, be familiar with relevant document types and standards, and demonstrate strong publishing, quality-control, organizational, and communication skills.

Skills

Clinical Trial Documentation
Electronic Case Report Forms
CRF and Annotated CRF
Define Documents
Clinical Study Data Reviewer’s Guide
Document Formatting and Publishing
Electronic Submission Readiness
Document Quality Control
Document Optimization
Naming Conventions
Document Review Tools
Issue Identification and Resolution
Attention to Detail
Time Management
Written and Verbal Communication
Teamwork

Visa sponsorship

Not detected in the job text

Keywords

Electronic Case Report Form
eCRF
Clinical Trial Documentation
CRF
Annotated CRF
aCRF
Define Documents
cSDRG
SDRG
Clinical Study Data Reviewer’s Guide
Electronic Submission Readiness
Document Publishing
Document Formatting
Document Standardization
Document Optimization
Quality Control
Document Review
Naming Conventions
Folder Structures
Clinical Research
Pharmaceutical Documentation
Submission Requirements
Document-Review Tools
Issue Resolution

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