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    • Interacts with internal and external groups to provide regulatory affairs consultative support for projects.
    • Initiates and manages regulatory affairs projects…
    • Vaccines (COVID-19 and others) are a requirement of the job unless you have an exemption on a medical ground pursuant to the Ontario Human Rights Code.
    • 3–5 years of experience reviewing medical and medico-legal reports.
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    • Support continuous improvement initiatives related to executive administration, physician affairs, organizational reporting, and operational effectiveness.
    • The base salary will be $76,490 - $109,190 per annum.
    • Starting salary will be aligned with the successful candidate’s experience, skills, and demonstrated…
    • Exposure to medical sciences and/or the pharmaceutical industry.
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    • Research experience in biomedical sciences, clinical research and/or medical devices.
    • Grants Development Consultant, Lawson - 1 position.
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    • The National Lead, Access and Public Affairs - West is responsible for activities related to improving access to CSL's portfolio in the Western provinces.
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Job Post Details

Nutrasource logo

Senior Regulatory Affairs Associate - job post

Nutrasource
120 Research Lane, Guelph, ON
$75,000–$100,000 a year - Full-time

Job details

Pay

  • $75,000–$100,000 a year

Job type

  • Full-time

Location

120 Research Lane, Guelph, ON

Full job description

Position Overview

Our rapidly expanding team is seeking a Senior Regulatory Affairs Associate to support regulatory sciences and clinical operations teams located in Guelph, ON. The Senior Regulatory Affairs Associate will provide leadership and support for various regulatory projects. The main responsibilities of the successful candidate will include the oversight and preparation of various regulatory submissions to support clinical trials and market access while ensuring compliance with applicable global policies, procedures, and regulatory guidelines.

Primary Responsibilities:

· Preparation and oversight of regulatory submissions and related documentation to primarily Health Canada, including Natural Health Product (NHP) Clinical Trial Applications (CTAs), Master Files, and Product License Applications (PLA), according to current Agency requirements.

· Interacts with internal and external groups to provide regulatory affairs consultative support for projects.

· Initiates and manages regulatory affairs projects to ensure content complies with emerging or new requirements.

· Identifies gaps in submission dossier to meet local requirements.

· Leads and provides guidance in the development and implementation of regulatory strategies.

· Liaises with functional areas to coordinate and compile information required for regulatory documentation.

· Interprets and makes decisions relating to regulatory guidelines and policies.

· Advises management on changes to regulations, standards and legal stipulations, and ensures SOPs and Work Instructions are updated to reflect such changes.

· Liaises with Health Canada and other regulatory agencies, as needed.

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

· Maintains positive and cooperative communications and collaboration with all internal and external stakeholders.

Core Competencies:

· Knowledge and experience in the Natural Health Products Regulations, associated regulatory principles, processes, and industry standards.

· Excellent communication skills with an ability to translate regulatory and scientific complexities into actionable guidance.

· Strong understanding of safety and efficacy evaluations.

· Excellent organizational time management and communication skills.

· Excellent interpersonal and public relation skills with ability to work well in a team.

· Solid problem-solving skills with an ability to identify solutions to problems under critical deadline constraints.

· Strong technical writing skills, and ability to review and critique regulatory documents.

· Ability to work independently with efficiency and accuracy and high attention to detail.

· Computer literacy with MS Office and Adobe Acrobat.

Qualifications:

· Advanced degree in a scientific discipline such as Pharmacology, Toxicology, Nutrition Science, Biochemistry, Regulatory Science, or related field.

· 8+ years of increasing responsibility in Regulatory Affairs/Regulatory Sciences for natural health products, supplements, OTCs, or similar regulated sectors.

· Proven experience preparing and submitting Class I–III NHP applications.

Pay: $75,000.00-$100,000.00 per year

Work Location: In person

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