Associate Site Manager (Clinical Research Associate) - Western Canada

Johnson & Johnson; Remote; CAD 55,000 - 75,000; Full time

Job summary

A leading healthcare company in Canada is seeking a Clinical Operations Associate to manage study sites and implement patient recruitment strategies. The ideal candidate will hold a Bachelor of Science or comparable degree and have at least one year of relevant experience. This role offers remote work flexibility and opportunities for career advancement, making it an excellent opportunity for those passionate about contributing to life-saving technologies.

Benefits

Competitive salary

Career advancement opportunities

Flexible work environment

Qualifications

• Minimum of 1 year experience in onsite and offsite monitoring.
• Knowledge of Good Clinical Practice and ICH guidelines.

Responsibilities

• Serve as the primary point of contact for study sites.
• Identify and implement patient recruitment strategies.
• Monitor study/site compliance with GCP standards.

Skills

Strong communication skills

Patient recruitment strategies

Site management

Education

Bachelor of Science, R.N., or equivalent

Job description

Employer Industry: Healthcare Innovation

Why consider this job opportunity:

• Opportunity to work with a leading employer in healthcare innovation
• Competitive salary with additional benefits
• Chance to contribute to the development of life‑saving medicines and treatments
• Remote work flexibility with the potential for travel within Canada
• Collaborative work environment with a focus on patient‑centered solutions
• Opportunity for career advancement within the Global Clinical Operations team

What to Expect (Job Responsibilities):

• Serve as the primary point of contact for study sites and liaise with study teams
• Actively identify and implement patient recruitment strategies at assigned sites
• Monitor study/site compliance with GCP standards and employer SOPs, both on‑site and remotely
• Provide site training to ensure adherence to regulations and trial‑specific procedures
• Resolve site‑specific issues in collaboration with investigators and site staff

What is Required (Qualifications):

• Bachelor of Science, R.N., or equivalent degree in Biological Sciences preferred
• Minimum of 1 year experience in onsite and offsite monitoring; other relevant experiences will be considered
• Knowledge of Good Clinical Practice, ICH guidelines, and local regulatory requirements
• Strong communication and influencing skills for effective site management
• Ability to establish a home office and work independently

How to Stand Out (Preferred Qualifications):

• Experience in pharmaceutical industry clinical research trials
• Analytical/risk‑based monitoring experience
• Knowledge of therapeutic areas, preferably including oncology
• Familiarity with clinical trial tracking systems and databases
• Fluent in English