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Remote Summer Writing Jobs in Quebec (NOW HIRING)

Study Report Support * Assist medical director(s) and/or technical writers by preparing statistical ... Summer Hours Program * Work Abroad Program - enjoy up to 4 weeks per year of remote work outside ...

Study Report Support * Assist medical director(s) and/or technical writers by preparing statistical ... Summer Hours Program * Work Abroad Program - enjoy up to 4 weeks per year of remote work outside ...

Study Report Support * Assist medical director(s) and/or technical writers by preparing statistical ... Summer Hours Program * Work Abroad Program - enjoy up to 4 weeks per year of remote work outside ...

Remote Summer Writing information

What is the difference between Remote Summer Writing vs Remote Summer Content Creation?

AspectRemote Summer WritingRemote Summer Content Creation
CredentialsWriting samples, basic writing skillsWriting samples, multimedia skills optional
Work EnvironmentHome-based, flexible hoursHome-based, flexible hours
Industry UsagePublishing, education, marketingMarketing, social media, digital media

Remote Summer Writing focuses primarily on producing written content such as articles, essays, or reports, often requiring strong writing skills. Remote Summer Content Creation includes writing but also involves creating multimedia content like videos or graphics. Both roles are flexible, home-based, and used across similar industries, but their core tasks differ in scope and skill set.

What are popular job titles related to Remote Summer Writing jobs in Quebec? For Remote Summer Writing jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Remote Summer Writing jobs in Quebec look for? The top searched job categories for Remote Summer Writing jobs in Quebec are:
What cities in Quebec are hiring for Remote Summer Writing jobs? Cities in Quebec with the most Remote Summer Writing job openings:

Statistician

Alimentiv

Sherbrooke, QC • Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 9 days ago


Job description

Responsible for the application of biostatistical methods to support clinical trials and data management, including statistical planning, design, analysis, and reporting throughout the project life cycle in accordance with project, organizational and regulatory standards.  Act as subject matter expert, providing statistical support to project teams, quality/study auditors, and external stakeholders. Participate in the promotion of Alimentiv as a global research organization, by contributing to the development, publishing, and reporting of project data. Please note we are hiring for multiple positions at this time.
Analysis Services
  • Carry out statistical analyses and provide direction to programmers, using standard software packages to interpret and translate results within a statistical framework into biomedical terms and prepare statistical data results for inclusion in reports and research papers that meet trial, organizational and regulatory best practices, and standards.
Academic Research Support
  • Working in conjunction with the Director of Academic Research, convert and present new and novel biometrical trial technologies, processes and findings into publishable and promotable scientific processes and results.
Project Support
  • Provide statistical expertise and guidance based on established methodologies throughout the project life cycle in the areas of study policies, protocols, implementation timelines and processes, data interpretation and publication of results.
  • Work with data management team to ensure data captured incorporates and corresponds to project protocols and requirements.  
Statistical Analysis/Data Collection Planning
  • Prepare statistical analysis plan and oversee project data collection, management, and analysis with input from the project teams that incorporates the type of information collected, sample size, randomization procedures, table and listing shells, project statistical policies, protocols, and methodology to be used to appropriately translate scientific questions into statistical hypotheses.
Study Report Support
  • Assist medical director(s) and/or technical writers by preparing statistical section of study report, publications and/or presentations ensuring statistical analyses adheres to trial, sponsor, organizational and regulatory requirements, and best practices.
Qualifications
  • A minimum of a Bachelor's or Master's degree and a professional designation + 1-3 years of related experience.
 
Working Conditions
  • Home-based.
$78,000 - $130,000 a year
+ Annual Bonus - Target 8%
 

Extended Health Benefits:

  • Health
  • Drug
  • Dental
  • Vision
  • Out of Province/Country Emergency Health

Insurance & Protection:

  • Accidental Death & Dismemberment (AD&D)
  • Life Insurance for you and your family members
  • Short- and Long-Term Disability

Retirement Savings:

  • Group Retirement Savings Plan (7% employer match with 5% employee contribution)

Wellness & Lifestyle Perks:

  • Education Reimbursement of up to $1,050 CAD (or local equivalent) annually for eligible expenses
  • Summer Hours Program
  • Work Abroad Program - enjoy up to 4 weeks per year of remote work outside your home region
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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