Skip to main content
Post your resume and find your next job on Indeed!

Medical Writer jobs in Ontario

Sort by: -
    • Proficient knowledge of new product and process development, current regulatory issues and regulations in Canada and the U.S. for NHPs/dietary supplements,…
  • View similar jobs with this employer
    • Accenture Song accélère la croissance et l'atteinte de la valeur ajoutée pour ses clients en leur assurant une pertinence durable auprès de leur clientèle.
  • View similar jobs with this employer
    • You are comfortable working with both qualitative and quantitative inputs, including conversations, interviews, survey data, partner insights, and performance…
    • Collaborative working style with experience briefing writers, partnering with art directors, and contributing to integrated creative ideation alongside strategy…
    • About Lockwood: Lockwood collaborates with clients in the pharmaceutical, biotech, and medical device industries to identify effective, holistic, science-based…
    • This craft blends imagination with strategy to create work that is emotionally resonant and culturally relevant.
    • A Quality Assurance Specialist/Medical proof reader will work with medical professionals submitting medical/legal reports to make sure that the final medical…
    • Regularly communicate medical insights from HCPs to inform and refine medical strategy and tactics.
    • Support the development and review of medical materials, as…
    • This role serves as the lead medical writer for assigned clients, brands, or therapeutic areas and contributes to additional projects as required.
    • 5+ years of experience as a medical writer in the sponsor and/or CRO setting.
    • BS degree or equivalent in a scientific or medical discipline with relevant…
    • Coach Associates and Specialists on process fundamentals to the medical team.
    • Adept at medical content research, distillation, and copywriting.
    • This role is well suited for an experienced medical affairs or medical communications professional who combines strong scientific expertise with emerging people…
    • This role is ideal for an experienced medical affairs or medical communications professional with deep scientific expertise, strong strategic leadership…
    • Exposure to regulated environments (e.g., medical device, pharma).
    • Serve as a scientific resource to internal stakeholders by providing research-based insights…
    • Minimum 4 years of regulatory medical writing experience.
    • At least 2 years as a medical writing project lead.
    • Interpreting clinical data and translating results…
Get email updates for the latest Medical Writer jobs in Ontario

By creating a job alert, you agree to our Terms . You can change your consent settings at any time by unsubscribing or as detailed in our terms.

People also searched:

medical writing
remote medical writer
scientific writer
scientific writing
remote pharmacist
writing
medical assistant
medical office
medical office assistant
medical receptionist

Career Resources:

Job Post Details

Regulatory Affairs Associate - job post

Nutrasource
120 Research Lane, Guelph, ON
$46,563.40–$60,000.00 a year - Full-time

Job details

Pay

  • $46,563.40–$60,000.00 a year

Job type

  • Full-time

Location

120 Research Lane, Guelph, ON

Full job description

The Regulatory Affairs Associate works in a cross-functional project environment to support assessment of products against regulatory frameworks and registration of products in North America.

Primary Responsibilities

· Compiles regulatory applications (primarily for Health Canada and the FDA) to achieve departmental and organizational objectives.

· Prepares regulatory documentation as appropriate in accordance with product classification and associated regulatory pathways (e.g., OTC/Pharmaceutical Drugs, Food Ingredients, Natural Health Products (NHPs)/Dietary Supplements, Veterinary Health Products, Cosmetics, Medical Devices).

· Supports literature reviews and drafting of safety and efficacy data.

· Supports reviews of product and manufacturing changes for compliance with applicable regulations.

· Keeps abreast of domestic and global regulatory trends, laws, and movements

Core Competencies

· Proficient knowledge of new product and process development, current regulatory issues and regulations in Canada and the U.S. for NHPs/dietary supplements, prescription and non-prescription drugs, biologics, and medical devices preferred;

· Excellent oral and written communication, including technical writing skills and the ability to review and critique regulatory documents

· Ability to work well within a team and as an individual contributor.

· Computer literacy with MS Office Suite

Qualifications

· Bachelor’s Degree in a scientific discipline

· Minimum of 1-2 years industry experience, within the regulatory affairs function of a CRO/CPG/Pharmaceutical/Nutraceutical/Medical Device company

Pay: $46,563.40-$60,000.00 per year

Work Location: In person

Let Employers Find YouUpload Your Resume