Medical Monitor (Infectious Diseases) at PSI CRO

Warsaw, Masovian Voivodeship, Poland -

Full Time

Start Date

Immediate

Expiry Date

24 Mar, 26

Salary

0.0

Posted On

24 Dec, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Medical Input, Clinical Studies, Patient Safety, Medical Matters, Clinical Development Plans, Data Review, Safety Monitoring, Pharmacovigilance, Risk Identification, Mitigation Strategies, FDA Compliance, EMEA Compliance, ICH Guidelines, GCP Guidelines, Communication Skills, Analytical Skills

Industry

Pharmaceutical Manufacturing

Description

Company Description 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 reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications. At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally. We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. 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. Full-time employment based in Poland 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 and Polish Proficiency with MS Office applications Communication, presentation and analytical skills Problem-solving, team and detail-oriented

Responsibilities

Medical Monitors provide medical input to global clinical studies and advise teams and business partners, focusing on patient safety. They collaborate on clinical development plans and ensure compliance with protocols and regulations.