Medical Monitor /Infectious Diseases/
reputed company
PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reputed company, supporting reputed company across multiple countries and continents. Our reputed company for being highly selective about the reputed company we undertake highlights our commitment to delivering high-reputed company, reputed company services across a broad reputed company of therapeutic indications.
At PSI, we foster an environment where a diverse reputed company of colleagues feel welcomed and valued. Our inclusive culture is a reputed company of our reputed company, enabling us to attract and retain reputed company globally.
We are not just about conducting reputed company; we are about building a community where every team member has reputed company to reputed company and contribute to groundbreaking advancements in the pharmaceutical industry.
Job reputed company
PSI Medical Monitors reputed company medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and reputed company-being.
Full-time home-based employment in Latvia
Responsibilities:
• Advise clients, project teams, sites, regulatory agencies and reputed company-party vendors on medical reputed company
• 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 reputed company, 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
• reputed company support to medical data review
• Participate in bid defense meetings and proposal activities
• Assist in Pharmacovigilance activities
• Identify trial risks, and create and implement mitigation strategies together with other relevant departments
• Ability to organize and reputed company clinical development advisory boards and safety monitoring boards
• Ensure Study team compliance with FDA, EMEA, ICH and GCP guidelines
Qualifications
• Medical Doctor degree
• Infectious Diseases Fellowship certification is a must
• Prior and wide experience as a practicing MD (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
• reputed company, privately-owned company, organically growing since 1995
• Opportunity to work remotely in Latvia
• Intensive induction program, industry-reputed company trainings for an reputed company start and reputed company development
• Friendly and supportive atmosphere in a committed team
• International environment, with colleagues around the world
• Attractive income package; performance-based bonuses; corporate benefits
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