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

Medical Affairs jobs

Sort by: -
    • 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.
    • Vaccines 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.
    • The primary responsibility of this role is to review and finalize complex medico-legal…
    • Strong experience within medical affairs, medical strategy, dermatology, skincare, or healthcare-related environments.
    • French proficiency is a plus.
    • Exposure to medical sciences and/or the pharmaceutical industry.
    • Coordinate with clients, medical editors and internal team members for successful project…
    • Research experience in biomedical sciences, clinical research and/or medical devices.
    • The Grants Development Consultant effectively manages multiple external…
    • Experience working with people in a health care, academic, and/or research environment with knowledge of medical, clinical and research terminology.
    • View all Northern Health jobs - Prince George jobs - Research Assistant jobs in Prince George, BC
    • Salary Search: ASSISTANT, RESEARCH salaries in Prince George, BC
    • See popular questions & answers about Northern Health
    • To provide assistance to the Board of Directors and members of the Co-operative in managing their affairs.
    • Reporting to:* District Support Advisor (Arctic Co-op…
    • To give advice, assistance and training to the Board of Directors and members of the Co-operative in managing their affairs;
    • Maintain a valid drivers license;
    • Create or revise labelling artworks, including primary, secondary, and any packaging components.
    • Assist in creation and revision of Product Monograph for Health…
    • The individual will be responsible for managing all relationships with public & private payers, and other relevant stakeholders, in support of market access…
  • View similar jobs with this employer
    • As the unified voice of the medical profession in the province, the SMA advocates on behalf of its members and engages in negotiations for physicians operating…
    • Assurer les communications entre les différents intervenants du GMF.
    • Rédiger, diffuser et assurer le suivi des communications destinées aux médecins et aux…
    • Se joindre à Puzzle Medical, c’est faire partie d’une équipe engagée à améliorer le traitement de l’insuffisance cardiaque avancée.
    • Options d'Achats d'Actions.
Get e-mail updates for the latest Medical Affairs jobs

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 science liaison
medical writer
medical affairs associate
medical office assistant
medical receptionist
business operations
corporate affairs
medical assistant

Career Resources:

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

Let Employers Find YouUpload Your Resume