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Medical Review Officer jobs in Ontario

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    • Prepare clinical trial submission dossiers for Regulatory and Ethics Authorities, with a specific focus on Canadian and US regulatory submissions, including…
    • Liaise with medical, clinical, data management, regulatory and QA personnel regarding safety issues, as appropriate.
    • RN + 10 yrs. relevant experience.
    • Peel Public Health has a strong track record of pioneering ideas that meet community needs.
    • Champion the Peel Public Health Strategic Plan, advancing health…
    • Strong expertise in the medical sciences, clinical development, medical program designing including experience in designing , executing and reporting of…
    • Conduct periodic meetings and performance reviews with medical personnel.
    • Lead the development, implementation, review, and continuous improvement of medical…
    • Chez Skyservice, nous continuons de croître et de fournir un service de haute qualité à nos clients, d’étendre notre empreinte et notre nom en Amérique.
    • As expert you will bring a deep technical mastery of the process and equipment.
    • That expertise allows you to lead the planning, process development and…
    • MRO Sales Manager will be responsible for developing, generating and administering MRO Sales and MRO customer relationships and will be reporting to the MRO…
    • These supports include but are not limited to: posting and communicating useful information about research, support during the pre and post award processes,…
    • The Department of Medicine and the Division of Cardiology at the University of Ottawa Heart Institute (UOHI) and The Ottawa Hospital are seeking a full-time…
    • Also required are a record of peer-reviewed research, and leadership in undergraduate, postgraduate, fellowship, continuing medical education or patient…
    • This position is responsible for managing the flow of Maintenance, Repair, and Operations (MRO) spare parts through the Parts Room.
    • Excellent verbal and written medical communication skills.
    • As a Medical Director, you will provide medical monitoring for assigned projects, function as medical…
    • This role is ideal for a detail-oriented operations professional who thrives in a fast-paced aviation maintenance environment.
    • Shift: Days – Monday to Thursday 7:30 am – 4 pm, Friday 7:30 am – 12:30 pm.
    • Must be able to meet Services Canada CGP requirement to a NATO level clearance.
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Job Post Details

Regulatory Officer - job post

PSI CRO
3.3 out of 5 stars
Mississauga, ON•Remote
$70,000–$90,000 a year - Full-time

Job details

Pay

  • $70,000–$90,000 a year

Job type

  • Full-time

Full job description

Company Description


We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 3,200 driven, dedicated and passionate individuals. We work on the front line of medical science, changing lives, and bringing new medicines to those who need them.


Job Description


Join our team of experts in regulatory and ethics submissions of clinical studies. You will focus on facilitating the start of research projects of novel medicinal products, while taking a step further in your professional career.

Your role:

  • Prepare clinical trial submission dossiers for Regulatory and Ethics Authorities, with a specific focus on Canadian and US regulatory submissions, including Import and Export license applications
  • Communicate with regulatory authorities, ethics committees, project teams and vendors on regulatory-related matters
  • Review translations of essential documents subject to clinical trial submission.
  • Track the regulatory project documentation flow
  • Review documents to greenlight IP release to sites
  • Manage safety reporting to authorities
  • Deliver regulatory training to project teams
  • Assist with feasibility research and business development requests

Qualifications
  • College/University degree or an equivalent combination of education, training and experience
  • Prior experience with clinical trial submissions in North America.
  • Full working proficiency in English and French, native French speaker competency required, US Spanish speaker competency beneficial.
  • Proficiency in MS Office applications
  • Detail-oriented
  • Ability to learn, plan and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
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