Clinical Research Associate

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 Fulfill other duties as required and requested by the company 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 Ability to travel for site visits, monitoring visits, SIVs, and investigator interactions up to 60% of the time within Canada and United States. 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. Actual 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.

The Clinical Research Associate is responsible for executing clinical operations activities including site management, monitoring visits, and Trial Master File maintenance. They must ensure study data integrity, compliance with GCP guidelines, and effective communication with study personnel to meet business objectives.

Candidates must hold a Bachelor’s degree in biomedical sciences, with a Master’s degree preferred. A minimum of 1-3 years of experience in clinical trials and proficiency in GCP guidelines and regulatory requirements are required.

• Group RRSP • Medical benefits

Identified from the job description. Confirm important requirements above.

• Clinical research
• Site management
• Trial master file maintenance
• Source data verification
• GCP guidelines
• Regulatory compliance
• Adverse event reporting
• Data management
• Quality management
• Protocol execution
• Risk mitigation
• Contract management
• Budget management
• Site initiation visits
• Monitoring visits
• Interpersonal communication
• Energetic
• Accountability
• Business Objectives
• Results Orientation
• Ethical Standards And Conduct
• Biomedical Sciences
• Management
• Clinical Research
• Clinical Trials
• Textiles
• Communication
• Critical Thinking
• Data Management
• Medical Ultrasonography
• Feedback Control
• Good Clinical Practices (GCP)
• Innovation
• Operations
• Prostate Cancer
• Quality Management
• Research Experiences
• Trial Master File
• Process Improvement
• Detail Oriented

• Science & Research
• Healthcare
• Engineering
• Clinical Research Associate
• Biologists, Botanists, Zoologists and Related Professionals
• Clinical Research Coordinators
• Natural Sciences Managers

Minimum education

Professional degree

Minimum experience

2+ years

Posting language

English

Working hours

40 hours per week