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

Medical Research Associate jobs

Sort by: -
    • Our rapidly expanding team is seeking a Senior Regulatory Affairs Associate to support regulatory sciences and clinical operations teams located in Guelph, ON.
    • Prepare and Review research project.
    • Prepare research ethics applications and amendments.
    • Coordinate, track and facilitate project activities, towards achieving…
    • Nous nous spécialisons dans les activités liées à l’IRM à toutes les phases (I-IV) des essais cliniques de neurologie.
    • Anglais - Excellent oral et écrit.
    • Medical writing: 1 year (required).
    • Demonstrated clinical research experience and an ability to adhere strictly to research protocols and guidelines whilst…
    • HyperMabs Inc. *is a fast-growing biotechnology company focussed on research and development of novel treatments for diseases with high unmet medical need.
    • This position is ideal for a scientist who enjoys translating protein biochemistry and molecular biology into robust, reproducible assays that advance research…
    • Prior experience in research or clinical settings is preferred, particularly in healthcare or medical research environments.
    • Ability to learn new research software and procedures efficiently.
    • The primary role of the Research Assistant I includes patient screening and recruitment, as…
    • NeuroRx est un chef de file dans l'analyse avancée d'images cérébrales et la gestion de projets au service de l'industrie pharmaceutique et biotechnologique.
    • Minimum 3 years clinical research, with nursing or medical doctor experience.
    • Clinical research: 3 years (preferred).
    • 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.
    • Strong understanding of medical terminology and healthcare procedures.
    • Background in research or clinical studies is a plus.
    • This role combines hands-on research with research project coordination, providing the opportunity to contribute to both collaborative and independent research…
    • Support the CEG with identifying, developing and carrying out priority research projects.
    • Work closely with project team to develop and implement research plans…
    • The Associate Manager, Scientific Program Development – Global plays a pivotal cross-functional role at DECIEM, driving project management across all scientific…
Get e-mail updates for the latest Medical Research Associate 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:

research assistant
science
shoppers mall
associate dentist
associate lawyer
associate physician
investment associate
medical assistant
medical office assistant
medical receptionist

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