Medical Monitor (Infectious Diseases) at PSI CRO

Vienna, , Austria -

Full Time

Start Date

Immediate

Expiry Date

12 Apr, 26

Salary

90000.0

Posted On

12 Jan, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Medical Input, Clinical Studies, Patient Safety, Data Review, Regulatory Compliance, Pharmacovigilance, Risk Identification, Mitigation Strategies, Communication Skills, Analytical Skills, Presentation Skills, Problem-Solving, Team-Oriented, Detail-Oriented, MS Office Proficiency, Infectious Diseases Fellowship

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. 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 What We Offer Excellent working conditions Extensive training and a friendly team Opportunities for personal and professional growth Meaningful mission – be part of a clinical research organization that helps brining new medicines to the patients A fair and attractive salary and benefits package starting from EUR 90,000 gross. The precise salary depends on the specific qualifications and experience, and will be agreed upon on an individual basis.

Responsibilities

Medical Monitors provide medical input to global clinical studies and advise teams on medical matters while focusing on patient safety. They also collaborate on clinical development plans and ensure compliance with regulatory guidelines.