Senior Clinical Research Scientist

Profound Medical; Mississauga; On-site; CAD 80,000 - 120,000; Full time

Job summary

An innovative firm is seeking a Senior Clinical Research Scientist to lead initiatives in clinical trial data integrity and analysis. This role involves developing software tools for data visualization, drafting high-quality scientific documents, and ensuring compliance with regulatory standards. The ideal candidate will possess a PhD in a quantitative field, extensive experience in medical writing, and strong analytical skills. Join a dynamic team focused on transforming healthcare through cutting-edge research and technology. This is a unique opportunity to make a significant impact in the medical field while advancing your career in a collaborative environment.

Qualifications

• 5+ years of relevant professional experience in clinical research.
• Medical writing portfolio with first-author publications.
• Knowledge of Good Clinical Practice (GCP) guidelines.

Responsibilities

• Develop and drive initiatives related to clinical trial data integrity.
• Draft high-quality presentations, manuscripts, and reports.
• Ensure compliance with Good Clinical Practice (GCP) guidelines.

Skills

Medical Writing

Project Management

Analytical Skills

Communication Skills

Biostatistical Methods

Education

PhD in Quantitative Science or Engineering

Tools

Microsoft Office

Visual Basic

R Statistical Software

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 Senior Clinical Research Scientist is accountable for developing and driving initiatives related to clinical trial data integrity, analysis, and reporting/publication. The role will coordinate relevant activities within a cross-functional team and drive high-quality results to on-schedule completion.

Duties and Responsibilities:

• Inform and execute the publication strategy for utilization and reimbursement
• Develop software tools to extract, analyze and visualize clinical data and perform critical interpretation
• Draft and revise high-quality presentations, manuscripts, abstract and reports and conduct scientific literature searches, data summaries, and systematic reviews
• Provide clinical leadership for regulatory reporting and new submissions
• Proactively identify gaps, and create and execute workflows related to clinical data integrity and analysis
• Advise marketing team on TULSA market positioning, and produce competitive assessment reports and briefings as needed
• Remain abreast of advancements in the standard of care and emerging trends; anticipate future challenges and opportunities
• Perform competitive analyses and develop strategic responses to support the adoption of TULSA
• Process treatment data in compliance with all applicable regulations
• Ensure compliance with Good Clinical Practice (GCP) and other relevant guidelines
• Fulfill other duties as required to support the Clinical Science team

Education and Certification:

• PhD degree in a quantitative science or engineering

Key Attributes (experience, skills and technical knowledge):

• >5 years relevant professional experience
• Medical writing portfolio including first-author publications
• Strong project management and organization skills
• Proactive, self-directed approach toward anticipating project needs and strong initiative to define and action clear next steps
• Ability to navigate complexity both independently and as part of a cross-disciplinary team in a fast-paced environment
• Exceptional analytical and critical thinking skills with strong attention to detail
• Exceptional oral and written communication skills
• Knowledge of biostatistical methods and systematic literature reviews
• Proficiency in Microsoft Office, Visual Basic, and R Statistical Software
• Knowledge of Good Clinical Practice (GCP) guidelines is an asset

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

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.