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 Italy or office based/hybrid in Milan
Responsibilities:
- Advise clients project teams sites 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
- Provide 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 lead 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 :
- Stable privately-owned company organically growing since 1995
- Comfortable office facilities with easy commute; opportunities to work office-based/hybrid/remote
- Intensive induction program industry-related trainings for an optimal start and continuous development
- Friendly and supportive atmosphere in a committed team
- International environment with colleagues around the world
- Attractive income package; performance-based bonuses; corporate benefits
Remote Work :
Yes
Employment Type :
Full-time
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 Italy or office based/hybrid in MilanResponsibilities:Advise clients project teams sites regulatory agencies and thir...
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 Italy or office based/hybrid in Milan
Responsibilities:
- Advise clients project teams sites 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
- Provide 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 lead 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 :
- Stable privately-owned company organically growing since 1995
- Comfortable office facilities with easy commute; opportunities to work office-based/hybrid/remote
- Intensive induction program industry-related trainings for an optimal start and continuous development
- Friendly and supportive atmosphere in a committed team
- International environment with colleagues around the world
- Attractive income package; performance-based bonuses; corporate benefits
Remote Work :
Yes
Employment Type :
Full-time
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