Clinical Research Study Assistant — PK Team (Flexible)

SmartRecruiters, Inc.; Toronto; On-site; CAD 54,000 - 67,000; Full time

Benefits offered by this job

HOOPP pension plan

Transit access

Flexible work environment

On-site gym discounts

Job summary

The University Health Network (UHN) seeks a dedicated Clinical Research Study Assistant to join the PK Team. This full-time role supports translational cancer research via biospecimen management and data quality, reporting to the Senior Manager, CSP.

Responsibilities include venipuncture, sample handling, data entry, and regulatory compliance, with opportunities to collaborate across oncology and clinical trials teams at the Princess Margaret Cancer Centre.

Qualifications

• Completion of a health-related community college diploma or equivalent is required.
• A bachelor’s degree or recognized equivalent in a health-related discipline is preferred.
• Strong communication, organizational, time-management and problem-solving skills.
• Ability to work under pressure and manage multiple tasks.

Responsibilities

• Perform venipuncture, vital signs assessments and ECG procedures per study protocols.
• Coordinate timed blood sampling and assessments with healthcare teams.
• Facilitate patient flow through clinical trial stages.
• Order, prepare and manage biospecimen collection kits.
• Document procedures in the electronic medical record (Epic).
• Maintain study documents, databases and equipment maintenance records.
• Apply QA procedures to ensure accurate and high-quality data.
• Interpret and adhere to applicable clinical research regulations.

Skills

Venipuncture

ECG

Vital signs assessments

Communication

Organizational skills

Time management

Problem solving

Teamwork

Customer service oriented

Education

Health-related college diploma

Bachelor’s degree preferred

Tools

MS Office

EPIC EMR

Job description

The University Health Network (UHN) seeks a dedicated Clinical Research Study Assistant to join the PK Team. This full-time role supports translational cancer research via biospecimen management and data quality, reporting to the Senior Manager, CSP.

Responsibilities include venipuncture, sample handling, data entry, and regulatory compliance, with opportunities to collaborate across oncology and clinical trials teams at the Princess Margaret Cancer Centre.