Toronto On Clinical trial startup Jobs – 9 Openings This Week

Clinical Research Associate
Profound Medical —Mississauga, ON
- $60,000–$75,000 a year
- Full-time
- Master's degree
- Bachelor's
- Continuous improvement
Clinical Coordinator
Tiny Health —Toronto, ON
- Full-time
- Remote
- Bachelor's
- Organizational skills
- Pediatrics
Quick apply
14d
Lead Clinical Research Associate
PSI CRO —Toronto, ON
- $124,000–$153,000 a year
- Full-time
- Remote
- English
- Microsoft Office
- Bachelor's
Quick apply
Senior Clinical Trial Analytics Monitor I
Everest Clinical Research —Markham, ON
- $100,000–$120,000 a year
- Remote
- Computer science
- Business development
- Project management
- Disability insurance
- Dental care
Quick apply
Sr. Clinical Operations Lead (Clinical Trial Manager)
Alimentiv —Toronto, ON
- $78,000–$130,000 a year
- Full-time
- Remote
- Microsoft Office
- Bachelor's
- Mentoring
Quick apply
Vice President, Clinical Operations
Sitero LLC —Mississauga, ON
- Full-time
- Hybrid work
- Master's degree
- Business development
- Bachelor's
- Paid time off
Quick apply
Applied Data Scientist, Health AI Evaluation & Datasets
Innodata Inc. —Toronto, ON
- $210,000–$240,000 a year
- Remote
- Medicine
- Doctoral degree
- Computer Science
Quick apply
Clinical Data Collection Manager
Oncoustics —Toronto, ON
- Full-time
- Master's degree
- Databases
- Project management
Regional Project Lead
PSI CRO —Toronto, ON
- $140,000–$155,000 a year
- Full-time
- Remote
- Customer service
- English
- Microsoft Office
Quick apply

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Senior Clinical Trial Analytics Monitor I
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Clinical Research Associate

Profound Medical -
Mississauga, ON

Apply Now

Job details

Full-time
$60,000–$75,000 a year

Qualifications

Data quality auditing
Clinical research
Quality management
Master's degree
Bachelor's
Data management
Continuous improvement
Risk management
Written report writing
Contracts
Good Clinical Practice (GCP)
Root cause analysis
Communication skills
Project progress tracking
Business process improvement

Full job description

Our mission is to Profoundly change the standard of care by creating a tomorrow where clinicians can confidently ablate tissue with precision; a tomorrow where patients have access to safe and effective treatment options, so they can quickly return to their daily lives. Changing the standard of care is part of our fabric. We are a group of energetic, problem-solvers focused on innovation, and looking to change the world. We are changing the paradigm for treating diseases such as prostate cancer by using real-time MR Imaging, thermal ultrasound and close-loop temperature feedback control, to gently ablate the diseased tissue with minimal side effects.

If you share our values and want to work in a collaborative results focused culture and want to make a Profound impact in healthcare and your career, here is your chance.

General Accountability:
The Clinical Research Associate will be responsible for analyzing, questioning, and improving how work gets done while demonstrating strong foundational CRA capabilities, meeting business objectives through efficient, quality trial execution from startup to closeout.

Duties and Responsibilities

Execute core clinical operations activities with attention to both detail and underlying context: site management, SIV, IMV, closeout visits, Trial Master File (TMF) maintenance, etc
Participate in review of site contracts, budgets, and ethics board submissions
Build and maintain effective relationships with study personnel
Investigate issues independently, identify root causes, and propose solutions
Ensure study data are accurate, complete, and verifiable through source data review/verification (SDR/SDV) by on-site, remote, or centralized monitoring activities
Analyze site and study data to identify inconsistencies, trends, or potential risks and develop mitigation strategies
Engage sites as a thought partner to improve protocol understanding and execution
Communicate findings, issues, and recommendations in a clear, structured, concise, and results-generating manner
Maintain TMF documentation that is clear, logical, compliant, and inspection-ready
Continuously seek opportunities to improve processes, clarity, and efficiency
Ensure that the study conduct, TMF, and adverse event reporting are compliant with the ethics board approval, Good Clinical Practice (GCP) guidelines, and all applicable local regulatory requirements
Conduct training for colleagues or study team as requested

Education

Bachelor’s degree in biomedical sciences required. MSc (thesis-based preferred) or equivalent research experience.

Certifications

SOCRA/CCRP or ACRP certification preferable/ completion of a clinical research graduate certificate.

Key Attributes

Ability to think critically beyond following process
Minimum of 1 - 3 years of experience
Strong written communication skills that are clear, concise, and logical
High level of initiative, ownership, and work ethics
Ability to structure and present information clearly
Attention to detail combined with big-picture thinking
Experience in administering and conducting clinical trials from startup to closeout
Proficiency in GCP guidelines, ethics board policies, applicable regulatory requirements, and all related processes
Proven ability to establish and maintain relationships with study site personnel
Proficiency in data management and quality management
Knowledge of adverse event reporting procedures and applicable regulatory requirements
Experience in conducting site initiation visits, monitoring visits, and close-out visits - both on-site and remotely
Outstanding interpersonal and communication skills
Ability to manage multiple tasks simultaneously, track project milestones, and ensure timely delivery of results
Strong attention to detail
Strong ability to work both independently and collaboratively

We thank you for your interest in Profound Medical. Please note only candidates that are short-listed will be contacted.

The expected annual salary range for this role is $60,000 - 75,000 CAD. A ctual compensation will be determined based on experience, qualifications, and job-related factors. This role may also be eligible for participation in the company’s benefits programs, such as a group RRSP and medical benefits paid by the employer .

We strive to promote diversity and equal opportunity in the workplace and encourage applications from all qualified individuals, including those with disabilities. If selected to participate in the recruitment, selection, and/or assessment process, please inform Human Resources of the nature of any accommodation(s) that you may require.

Apply Now

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clinical trial startup jobs in toronto on

Clinical Research Associate

Clinical Coordinator

Lead Clinical Research Associate

Senior Clinical Trial Analytics Monitor I

Sr. Clinical Operations Lead (Clinical Trial Manager)

Vice President, Clinical Operations

Applied Data Scientist, Health AI Evaluation & Datasets

Clinical Data Collection Manager

Regional Project Lead

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