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Clinical Operations Jobs in Ontario (NOW HIRING)

destinationone Consulting

Manage day-to-day clinical operations and staff performance. Collaborate with healthcare professionals to develop care protocols. Monitor patient outcomes and implement quality improvement ...

Sitero LLC

Senior Clinical Trial Manager

Markham, ON · On-site

Clinical Operations ESSENTIAL DUTIES AND RESPONSIBILITIES: The Clinical Trial Manager (CTM) will oversee one or more clinical trials and ensure that project milestones are met on time, within budget ...

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All JobsClinical Operations JobsClinical Operations Jobs in Ontario

Clinical Operations information

See Ontario salary details

$29K

$101.8K

$205K

How much do clinical operations jobs pay per year?

As of Aug 29, 2026, the average yearly pay for clinical operations in Ontario is $101,829.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,000.00 and $128,500.00 per year, depending on experience, location, and employer.

What is clinical operations?

Clinical operations refers to the planning, management, and execution of clinical trials and research studies within the healthcare and pharmaceutical industries. Professionals in clinical operations ensure that studies are conducted efficiently, ethically, and in compliance with regulatory requirements. Their responsibilities may include site management, patient recruitment, data collection, and ensuring protocol adherence. The goal is to facilitate the safe and effective development of new medical treatments and therapies.

How does a clinical operations professional typically collaborate with cross-functional teams during a clinical trial?

Clinical Operations professionals play a central role in coordinating activities among various teams such as regulatory affairs, data management, biostatistics, and clinical research associates. They ensure that timelines are met, protocols are followed, and all departments are aligned with trial objectives. Regular meetings, clear communication, and the ability to anticipate and resolve operational challenges are essential to successful collaboration. This cross-functional teamwork helps maintain trial quality and regulatory compliance throughout the study.

What are the key skills and qualifications needed to thrive in clinical operations, and why are they important?

To thrive in Clinical Operations, you need expertise in clinical trial management, regulatory compliance, and data analysis, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) certification, and electronic data capture (EDC) platforms is essential. Strong leadership, problem-solving, and communication skills help coordinate teams and ensure project timelines are met. These skills are crucial for guaranteeing efficient, compliant, and successful clinical trial execution in a highly regulated environment.

What is the difference between Clinical Operations vs Clinical Research Associate?

AspectClinical OperationsClinical Research Associate
Required CredentialsBachelor's degree, experience in clinical trial managementBachelor's degree, often with certification in clinical research
Work EnvironmentProject management, coordinating multiple trial sitesMonitoring clinical sites, ensuring protocol compliance
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, pharmaceutical companies
Common Search & ComparisonFocuses on trial oversight and managementFocuses on site monitoring and data verification

Clinical Operations professionals oversee the planning, coordination, and management of clinical trials, ensuring they run smoothly across multiple sites. Clinical Research Associates primarily monitor clinical trial sites, verify data accuracy, and ensure compliance with protocols. While both roles require knowledge of clinical research, Clinical Operations has a broader scope involving project management, whereas CRAs focus on site-level monitoring.

What are the most commonly searched types of Clinical Operations jobs in Ontario?

The most popular types of Clinical Operations jobs in Ontario are:

What are popular job titles related to Clinical Operations jobs in Ontario?

For Clinical Operations jobs in Ontario, the most frequently searched job titles are:

What job categories do people searching Clinical Operations jobs in Ontario look for?

The top searched job categories for Clinical Operations jobs in Ontario are:

Clinical Operations jobs near you
Infographic showing various Clinical Operations job openings in Ontario as of August 2026, with employment types broken down into 84% Full Time, 14% Part Time, and 2% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $101,829 per year, or $49 per hour.

Director Clinical Operations

Pharma Medica Research Inc.

Toronto, ON

Full-time

Medical, Vision, Life

Posted 13 days ago

Job description

Pharma Medica Research (PMRI) Inc. is a Contract Research Organization that strives for innovation and original solutions in a highly regulated and competitive industry. If your career goals align with innovation and original thinking you will be the perfect candidate to be part of an inclusive, adaptable, and forward-thinking organization. Our reputation for delivering high quality research is outstanding. At PMRI we are committed to making a difference in healthcare and people’s lives. Come join our team!


We are currently searching for a Director, Clinical Operations to join our Toronto Team! The Director, Clinic Operation plans, organizes and oversees the activities of Pharma Medica Research Inc. (PMRI) departments including kitchen, cleaning, clinic assistants, administration, clinic supplies and building management. The Director, Clinic Operations reports to the VP, Medical Affairs and/or designate.


Duties and Responsibilities:

  • Plan, organize and manage the operations of the following clinical areas of responsibility: kitchen, facility, clinic assistants, administration, clinic supplies, and building management.
  • Supervise the managers and supervisors from the above departments.
  • Consult with senior management to maintain and establish standards for the provision of clinic services.
  • Oversee the management for all clinic studies supplies and stock maintenance.
  • Ensure general clinic duties are performed to prepare for the clinical study (e.g., tube labeling, bunk room preparation, set up bleeding stations, etc.
  • Ensure all direct reports are specifically trained in all assigned tasks and duties.
  • Ensure all clinical and laboratory supplies are adequately stocked on site.
  • Provide necessary reports as defined by the President
  • Ensure Health and Safety rules and regulations are adhered to at all times.
  • Perform any tasks required by the President deemed necessary to conduct a clinical study.
  • Other duties as required.



Qualifications

  • MSc in Life Sciences or related field; CCRP Certification preferred.
  • Minimum 5 years of management experience in clinical research (preferably in a CRO setting).
  • At least 5 years in a leadership role.
  • Strong knowledge of GCP, ICH, FDA, and Health Canada regulations.
  • Proven ability in strategic planning, team leadership, and cross-departmental communication.
  • Excellent interpersonal and communication skills.
  • Strong computer skills in Microsoft Office Applications


We offer:

  • Competitive compensation plan
  • Mentorship Opportunities
  • A benefit plan that is fully paid for by PMRI, including healthcare, dentalcare, vision care, LTD, Life Insurance, AD&D, along with a Health Spending and Wellness Spending Accounts and a voluntary RRSP Contribution Plan
  • Opportunities for advancement and career progression
  • A generous Employee Milestones Awards Program
  • Corporate Discounts Program
  • Learning Support Programs
  • Friendly atmosphere, culture of learning

Please note all applications must be eligible to work within Canada.

PMRI is an Equal Opportunity Employer; promoting accessibility and inclusivity at work and offering accommodation for applicants as required and requested.

We thank all applicants for their interest; however, only those selected to proceed in the interview process will be contacted.

Apply