PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
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.
Home-Based in Canada
Responsibilities:
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.
Provides medical oversight for global clinical trials, serving as the medical and safety contact, monitoring participant well-being, advising study teams, and contributing gastroenterology expertise throughout trial delivery.
Provides medical oversight for global clinical trials, serving as the medical and safety contact, monitoring participant safety, reviewing trial data and documents, and advising teams on gastroenterology matters.
Provides medical oversight for gastroenterology clinical trials, monitoring participant safety, advising study teams on medical and safety questions, and supporting trial documentation, reviews, and regulatory responses.
Provide virtual, relationship-based primary care while supervising and developing Nurse Practitioners, improving clinical quality, and advancing population health and value-based care across patient panels.
The SERM Medical Director will lead safety evaluations and benefit-risk assessments for pharmaceutical products, ensuring compliance and effective risk management in clinical development and post-marketing settings.
