Clinical Research Coordinator - Phase 1 Group

Alberta Health Services; Edmonton; On-site; CAD 49,000 - 62,000; Full time

Benefits offered by this job

Health benefits

Job summary

Alberta Health Services seeks a Clinical Research Coordinator for the Phase 1 group at Cross Cancer Institute. You will support oncology trials, coordinate visits from site selection to close-out, manage regulatory documents, and liaise with sponsors and internal teams to ensure study conduct and data integrity.

Ideal candidates bring at least two years of clinical research experience, oncology knowledge, and proficiency with EMR systems and trial databases, with ICH-GCP training and

Qualifications

• Completion of a minimum two year diploma or certificate in a health care related field.
• Minimum of two years' clinical research experience.
• Oncology knowledge and general clinical trial experience required.
• Cancer/disease sites or Phase 1 trials experience is an asset.
• ICH-GCP training and familiarity with regulatory reporting requirements.
• Excellent computer skills; experience with Microsoft Office and databases.
• Experience with EMR systems (Netcare, ARIA, Connect Care) and ethics submission systems (IRISS, REMO).
• Ability to transport materials; physical tasks up to 40 lbs; multitasking in busy area.

Responsibilities

• Coordinate study visits from site selection to close-out.
• Maintain regulatory documentation and liaise with industry partners.
• Track workflows, data/ethics submissions, and study metrics.
• Review source documents and resolve data queries for trials.
• Assist with site audits and regulatory inspections as needed.

Education

Two-year health care diploma or certificate

Tools

InForm

RAVE

Netcare

ARIA

Connect Care

IRISS

REMO

Microsoft Office

Job description

Clinical Research Coordinator - Phase 1 Group

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 Phase 1 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
• Primary Location: Cross Cancer Institute
• Multi-Site: Not Applicable
• FTE: 1.00
• Posting End Date: 13-OCT-2026
• Temporary Employee Class: Temp F/T Benefits
• Date Available: 02-NOV-2026
• Temporary End Date: 01-NOV-2027
• 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

• Transition Company: Cancer Care Alberta
• Classification: Clinical Resrch Coord (ACB)
• Union: HSAA Facility PROF/TECH
• Unit and Program: Clinical Trials Unit
• Primary Location: Cross Cancer Institute
• Location Details: As Per Location
• Multi-Site: Not Applicable
• FTE: 1.00
• Posting End Date: 13-OCT-2026
• Temporary Employee Class: Temp F/T Benefits
• Date Available: 02-NOV-2026
• Temporary End Date: 01-NOV-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 all cancer/disease sites or Phase 1 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.

Please note:

All postings close at 23:59 MT of the postingend date indicated.

Security Screening:

A satisfactory criminal record check and/or Vulnerable Sector Search is required prior to your first day of work. Additionally, all employees have an ongoing duty to disclose any charges or convictions that may occur during their employment with AHS.

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