Associate Site Manager

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

R&D Operations

Job Sub Function:

Clinical Trial Support

Job Category:

Professional

All Job Posting Locations:

Toronto Ontario Canada

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.

Learn more at are searching for the best talent for an Associate Site Manager (Clinical Research Associate) Greater Toronto Area. This position is a field-based role covering primarily Ontario; occasional travel outside of this province as the Associate Site Manager should be located in the Greater Toronto Area

Purpose:

As an Associate Site Manager (Clinical Research Associate) you will be part of the Global Clinical Operations (GCO) Canada team and will be responsible for study site management through the assessment/selection initiation maintenance and closure phases of a clinical trial (Phase 1 4 trials).

You will be responsible for:

• You are the primary point of contact for the study site; liaison with study teams.
• Your responsibilities include actively identifying and driving patient recruitment strategies at assigned sites.
• You are responsible for monitoring the study/site according to GCP standards and J&J GCO SOPs both on-site and with remote contacts. This includes source document verification Investigator Site File (ISF) review and accurate drug accountability.
• You will provide site training during site initiation and ongoing to ensure compliance with all required regulations SOPs trial-specific tools and systems and specialized procedures.
• You will ensure resolution of site-specific issues and will partner closely with investigator and site staff to meet all study timelines.
• You will work closely with the local study operations team to resolve protocol and site-specific issues.
• You will use and maintain the clinical trial tracking system (CTMS) and update the electronic Trial Master File (TMF) as required.

Qualifications / Requirements:

• Bachelor of Science or equivalent degree in Biological Sciences required.
• Minimum of 1 year experience in onsite and offsite (remote) monitoring; however other relevant experiences and skills may be considered by the hiring manager when considering the candidates eligibility.
• Pharmaceutical industry clinical research trial experience preferred.
• Analytical/risk-based monitoring experience is highly preferred.
• Knowledge of several therapeutic areas is an asset (preferably including oncology).
• In-depth knowledge of Good Clinical Practice ICH guidelines and local regulatory requirements.
• Ability to operate and use various systems and databases (e.g. CTMS EDC TMF various dashboards/metrics IWRS safety reporting).
• Strong communication and influencing skills to effectively manage study sites both remotely and face-to-face.
• Strong team member and self-starter with the ability to work independently.
• Ability to establish a home office.
• Fluent in English language.
• Travel: 30-50%. Onsite monitoring visits will be conducted in combination with offsite (remote) monitoring visits. You will be assigned sites mainly within your region/province with occasional need for travel to neighboring provinces.

This job posting is anticipated to close on June 24th 2026. The Company may however extend this time-period in which case the posting will remain available on to accept additional applications.

The anticipated base pay range for this position is $72000 $116150 CAD.

The compensation and benefits information set forth in this posting applies to candidates hired in Canada. Candidates hired outside Canada will be eligible for compensation and benefits in accordance with their local market.

• Under current guidelines this position is eligible for a discretionary performance bonus.
• The Company uses AI in its assessment of applicants.
• This job posting is for an existing position.

#LI-Remote

Required Skills:

Preferred Skills:

Analytical Reasoning Business Behavior Business English Clinical Data Management Clinical Trials Clinical Trials Operations Execution Focus Issue Escalation Laboratory Operations Process Improvements Process Oriented Project Support Regulatory Environment Research and Development Research Ethics Study Management Time Management

The anticipated base pay range for this position is :

$72000 $116150 CAD

Additional Description for Pay Transparency:

Required Experience:

Manager

Employment Type : Full-Time
Experience: years
Vacancy: 1
Monthly Salary Salary: 72000 - 116150