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Medical Monitor (Board-Certified Oncologist) - Remote

Posted 9 weeks ago
All others
Full Time
Canada

Overview

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being.

In Short

  • Advise clients, project teams, sites, data safety monitoring boards, regulatory agencies and third-party vendors on medical matters
  • Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations
  • Review and analysis of clinical data to ensure the safety of study participants in clinical studies
  • Ensure that the reported data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments
  • Address safety issues across the study from sites and the study team
  • Review listings for coded events to verify Medical Dictionary for Regulatory activities
  • Participate in bid defense meetings
  • Assist in Pharmacovigilance activities
  • Identify Program risks, and create and implement mitigation strategies with Clinical Operations
  • Ability to organize and lead clinical development advisory boards and safety monitoring boards
  • Ensure Study team compliance with FDA, EMEA, ICH and GCP guidelines
  • Review and sign off clinical documents with respect to medical relevance.

Requirements

  • Medical Doctor degree required
  • Board Certification in Oncology required
  • Experience as a practicing Oncologist (minimum of 10 years)
  • Clinical Research experience required, such as experience as a Principal Investigator or Sub-Investigator
  • Full working proficiency in English
  • Proficiency with MS Office applications
  • Excellent communication and presentation skills, comfortable public speaking
  • Problem-solving, team and detail-oriented

Benefits

  • Join an international group of medical professionals
  • Build a career on the frontline of medical science
  • Use your knowledge and expertise to help bring new medications to patients
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PSI CRO

PSI CRO is a prominent Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Founded in Switzerland, PSI is a privately owned, full-service CRO that operates globally, supporting clinical trials across various countries and continents. The company is known for its selective approach to project engagement, emphasizing high-quality and timely services across a wide range of therapeutic areas. PSI values diversity and inclusivity within its workforce, fostering an environment where all colleagues feel welcomed and valued. The organization is dedicated to not only conducting clinical trials but also building a community that empowers team members to thrive and contribute to significant advancements in the pharmaceutical sector.

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