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Added 6 mins ago
AB
Operations Manager
Avis Budget Group
Ottawa, ON
- Full-time
Recent graduate with Bachelor's Degree OR High School diploma/GED plus at least 4 years supervisory experience OR Associate's Degree plus at least 2 years supervisory experience.
Added 6 mins ago
JI
Operations-Warehouse
J.D. Irving, Limited
Bouctouche, NB
- Full-time
Are you organized and detail-oriented, with a passion for logistics? Kent Homes is seeking a Warehouse Associate to support our operations in managing the flow of materials for modular…
Added 6 mins ago
JI
Project Sales Associate
J.D. Irving, Limited
Moncton, NB
- Full-time
Added 6 mins ago
JE
Production Associate
Johnson Electric
Ancaster, ON · Canada - PM Ancaster (General)
- Full-time
Join Our Team as a Rig Setup Production Associate at Johnson Electric!
Added 6 mins ago
TT
Assistant Store Manager Winners HomeSense Collingwood Centre
The TJX Companies, Inc.
Collingwood, ON
- Full-time
Immediate access to our Group Benefits package, including a Health Care Spending Account, Associate & Family Assistance Program, and various well-being resources
Added 21 mins ago
TT
Retail Store Associate Part Time Winners/HomeSense – Granite Plaza
The TJX Companies, Inc.
New Minas, NS
- Part-time
Support for you and your family through our Associate and Family Assistance programs, offering helpful resources and services to enhance your well-being.
Added 21 mins ago
SD
Merchandiser, Hourly Full Time Flexible Shifts
Shoppers Drug Mart
Saint John, NB
- Full-time
Each store has an Associate-Owner, so you will work for a local business owner while having the support of a national brand. Benefit from a purchase discount program, flexible and varied…
Added 21 mins ago
SD
Assistant.e technique en pharmacie, rémunéré(e) à l’heure – PHX temps plein Quarts de travail flexibles Embauche feu vert
Shoppers Drug Mart
Saguenay, QC
- Full-time
Work for a local business owner while having the support of a strong retail brand. Benefit from a purchase discount program, flexible and varied schedules, competitive pay and online…
Added 21 mins ago
SD
Merchandiser, Hourly Part Time Day
Shoppers Drug Mart
Toronto, ON
- Part-time
Each store has an Associate-Owner, so you will work for a local business owner while having the support of a national brand. Benefit from a purchase discount program, flexible and varied…
Added 21 mins ago
SD
Pharmacy Assistant, Hourly Part Time Evening
Shoppers Drug Mart
Newmarket, ON
- Part-time
Each store has an Associate-Owner, so you will work for a local business owner while having the support of a national brand. Benefit from a purchase discount program, flexible and varied…
Added 21 mins ago
SD
Pharmacy Assistant, Hourly Full Time Day Greenlight Requisition
Shoppers Drug Mart
Toronto, ON
- Full-time
Each store has an Associate-Owner, so you will work for a local business owner while having the support of a national brand. Benefit from a purchase discount program, flexible and varied…
Added 21 mins ago
SD
Pharmacy Assistant, Hourly Part Time Evening
Shoppers Drug Mart
Hamilton, ON
- Part-time
Each store has an Associate-Owner, so you will work for a local business owner while having the support of a national brand. Benefit from a purchase discount program, flexible and varied…
Added 21 mins ago
SD
Assistant Front Store Manager, Hourly Full Time Evening
Shoppers Drug Mart
Toronto, ON
- Full-time
Each store has an Associate-Owner, so you will work for a local business owner while having the support of a national brand. Benefit from a purchase discount program, flexible and varied…
Added 21 mins ago
SD
Technicien en pharmacie assujetti à une règlementation, rémunéré(e) à l’heure – PHX temps partiel Quarts de travail flexibles Embauche feu vert
Shoppers Drug Mart
Saguenay, QC
- Part-time
Work for a local business owner while having the support of a strong retail brand. Benefit from a purchase discount program, flexible and varied schedules, competitive pay and online…
Added 21 mins ago
SD
Regulated Pharmacy Technician, Hourly Part Time Day
Shoppers Drug Mart
St. Albert, AB
- Part-time
Each store has an Associate-Owner, so you will work for a local business owner while having the support of a national brand. Benefit from a purchase discount program, flexible and varied…
Added 21 mins ago
SD
Assistant.e technique en pharmacie, rémunéré(e) à l’heure – PHX temps partiel Quarts de travail flexibles
Shoppers Drug Mart
Montreal, QC
- Part-time
Work for a local business owner while having the support of a strong retail brand. Benefit from a purchase discount program, flexible and varied schedules, competitive pay and online…
Added 21 mins ago
SD
Merchandiser, Hourly Part Time Flexible Shifts
Shoppers Drug Mart
Toronto, ON
- Part-time
Each store has an Associate-Owner, so you will work for a local business owner while having the support of a national brand. Benefit from a purchase discount program, flexible and varied…
Added 21 mins ago
SD
Beauty Manager, Hourly Full Time Flexible Shifts
Shoppers Drug Mart
Grand Bend, ON
- Full-time
Work in conjunction with the Associate-Owner and Front Store Manager
Added 21 mins ago
Senior Customer Experience Associate - March Road, Kanata, ON - 18.75 hours/week
Scotiabank
Ottawa, ON · Kanata, ON
…conversations that enable faster advancement and internal training to support your growth and…
Added 21 mins ago
W
Full Time Asset Protection Associate - Security License Required.
Walmart
Chatham-Kent, ON
- Full-time
The Asset Protection Associate plays a key role in creating and maintaining a safe, secure, and professional store environment for customers, associates, visitors, and vendors. By following…
Added 21 mins ago
A
Associate Data Scientist
AlgaeCal
Remote, Canada
- $60,000 to $70,000 CAD / year
- Full-time
- Remote
AlgaeCal is looking for a top-tier Associate Data Scientist who can turn raw information into strategies that drive measurable results.
Added 21 mins ago
A
Associate Data Scientist
AlgaeCal
Remote, Canada
- $60,000 to $70,000 CAD / year
- Full-time
- Remote
AlgaeCal is looking for a top-tier Associate Data Scientist who can turn raw information into strategies that drive measurable results.
Added 21 mins ago
A
Associate Data Scientist
AlgaeCal
Remote, Canada
- $60,000 to $70,000 CAD / year
- Full-time
- Remote
AlgaeCal is looking for a top-tier Associate Data Scientist who can turn raw information into strategies that drive measurable results.
Added 21 mins ago
A
Associate Data Scientist
AlgaeCal
Remote, Canada
- $60,000 to $70,000 CAD / year
- Full-time
- Remote
AlgaeCal is looking for a top-tier Associate Data Scientist who can turn raw information into strategies that drive measurable results.
Added 21 mins ago
A
Associate Data Scientist
AlgaeCal
Remote, Canada
- $60,000 to $70,000 CAD / year
- Full-time
- Remote
AlgaeCal is looking for a top-tier Associate Data Scientist who can turn raw information into strategies that drive measurable results.

Alberta Health Services

Clinical Research Coordinator - Neuroendocrine

AB, Canada
Greater Edmonton Metropolitan Area, Canada

Temporary

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Job details

Job type: Temporary
Apply by: Dec 4, 2026
Posting language: English
Posted: Nov 4, 2026

Original job description

Your Opportunity:

Are you an experienced clinical trial professional looking to work with cutting-edge cancer therapies? We are seeking a dynamic Clinical Trials Coordinator to join our Clinical Trial Unit (CTU), with a primary assignment to the Neuroendocrine group. Reporting to the CTU Associate Manager, you will work in a team environment to facilitate clinical trial activities and complete delegated study tasks. While your daily focus will highlight ongoing study conduct, patient data management, and monitoring/inspection readiness, all coordinator positions maintain a general scope and may be reassigned to, or assist, other teams within the Unit as operationally required. Building strong relationships is key, as you will serve as a central study point of contact for PIs & study staff, internal CCI departments, outside hospitals, and external agencies (e.g., Sponsors, CROs, and Health Canada). Operationally, you will coordinate study visits - from site selection through to close-out - while managing regulatory documentation and liaising with industry partners for day-to-day study specifications. To ensure efficiency, you will create and update systems to track workflows, regulatory documentation, and data/ethics submissions. Responsibilities may also include reviewing source documents, abstracting protocol data to complete CRFs, and resolving data queries. You will track study metrics, coordinate monitoring visits, and assist with site audits and regulatory inspections. Additionally, you will manage patient study registration, notify personnel of assigned treatments, relay adverse drug reaction reports, and ensure all required safety documentation is completed. If you are a detail-oriented professional with a passion for oncology research, we want to hear from you!

Description:

As a Clinical Research Coordinator, you will provide support for research studies through the identification, collection, and reporting of clinical trial data. You will compile research, reports and regulatory documents as required by the protocol, and study/sponsor. This involves ensuring research information is timely, accurate, valid, meaningful, and to the sponsor's satisfaction, and that studies are run according to local and global regulations.

Transition Company: Cancer Care Alberta Classification: Clinical Resrch Coord (ACB) Union: HSAA Facility PROF/TECH Unit and Program: Clinical Trials Unit, Cancer Care Alberta Primary Location: Cross Cancer Institute Location Details: As Per Location Multi-Site: Not Applicable FTE: 1.00 Posting End Date: 12-NOV-2026 Temporary Employee Class: Temp F/T Benefits Date Available: 30-NOV-2026 Temporary End Date: 03-DEC-2027 Hours per Shift: 7.75 Length of Shift in weeks: 2 Shifts per cycle: 10 Shift Pattern: Days Days Off: Saturday/Sunday Minimum Salary: $35.34 Maximum Salary: $45.03 Vehicle Requirement: Not Applicable

Required Qualifications:

Completion of a minimum two year diploma or certificate in a health care related field. Minimum of two years' clinical research experience.

Additional Required Qualifications:

Oncology knowledge and general clinical trial experience required; experience with neuroendocrine cancer/disease or trials is an asset. Prior experience working with pharmaceutical sponsors. An ability to multi-task effectively in a busy area with multiple interruptions and competing demands. Knowledge of oncology medical terminology, anatomy and tumor staging. ICH-GCP training and familiarity with clinical trial regulatory reporting requirements. Excellent computer skills and experience working with Microsoft Office programs. Familiar with using and creating spreadsheets, and using various databases (e.g. InForm, RAVE). Experience with electronic medical records (e.g. Netcare, ARIA, Connect Care), and ethics submission systems (IRISS, REMO). Must be able to transport large volumes of materials (study supplies, charts, boxes, etc.) to various areas regularly and push/pull loaded carts. Physical demands of the job include sitting for extended periods, pushing heavy carts, lifting boxes of documents/office/medical supplies and equipment weighing up to 40 lbs., and using repetitive motions, lifting, bending, reaching and standing for prolonged periods. To ensure your skills and qualifications are considered, please attach a resume and cover letter with your application indicating how your education and experience meet the requirements of this position.

Preferred Qualifications:

Preference given to those with a bachelor’s level degree (health-related). Completion of an approved Clinical Research or Data Management Certificate Program. SoCRA or ACRP certification/membership.

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More about this job

Responsibilities

Coordinate clinical trial activities and study visits from site selection through close-out, while managing regulatory documents, study workflows, and communications with investigators, sponsors, CROs, and other partners. Collect and report accurate trial data, support patient registration and safety reporting, resolve data queries, track study metrics, and assist with monitoring visits, audits, and inspections.

Requirements

Requires a minimum two-year diploma or certificate in a healthcare-related field and at least two years of clinical research experience, including oncology knowledge, general clinical trial experience, and pharmaceutical sponsor experience. Candidates need ICH-GCP training, familiarity with regulatory reporting, oncology terminology and tumor staging, strong computer and database skills, and the ability to manage competing demands and physical tasks; a health-related bachelor's degree, clinical research or data management certificate, and SoCRA or ACRP certification or membership are preferred.

Skills

Clinical Trial Coordination
Oncology Research
Neuroendocrine Cancer
Clinical Data Management
Regulatory Documentation
ICH-GCP
Clinical Trial Regulatory Reporting
Source Document Review
Case Report Forms
Data Query Resolution
Monitoring Visit Coordination
Audit and Inspection Readiness
Patient Study Registration
Adverse Drug Reaction Reporting
Microsoft Office
Electronic Medical Records

Visa sponsorship

Not detected in the job text

Keywords

Clinical Trials Unit
Clinical Research
Oncology
Neuroendocrine Cancer
Clinical Trial Coordination
ICH-GCP
Regulatory Reporting
Clinical Trial Data
Case Report Forms
Source Documents
Data Queries
Study Monitoring
Regulatory Inspections
Clinical Audits
Adverse Drug Reactions
Microsoft Office
Spreadsheets
InForm
RAVE
Netcare
ARIA
Connect Care
IRISS
REMO
Pharmaceutical Sponsors
CROs
Health Canada
Tumor Staging
SoCRA
ACRP

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