Medical Monitor

il y a 3 jours


Leuven, Flandre, Belgique PSI CRO AG Temps plein

23 hours ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Company Description PSI is a leading Contract Research Organization with more than 25 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. Job Description 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. Responsibilities: Medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines 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, narratives, 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 Supports and/or performs medical data review of the operational clinical trial database Participate in meetings with clients and Investigators Assist in Pharmacovigilance activities Identify Program risks, and create and implement mitigation strategies with Clinical Operations 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 medically relevant documents. Qualifications Medical Doctor degree Oncology Fellowship certification is a must Prior and wide experience as a practicing Oncologist (minimum of 10 years) Full working proficiency in English Proficiency with MS Office applications Communication, presentation and analytical skills Problem-solving, team and detail-oriented Additional Information 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. Seniority level Mid-Senior level Employment type Full-time Job function Other Industries Pharmaceutical Manufacturing #J-18808-Ljbffr


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