Medical Monitor (Infectious Diseases).

PSI; Madrid; Híbrido; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A healthcare organization is seeking a Medical Monitor in Madrid or Barcelona to provide medical guidance for global clinical studies. In this role, you will advise clients, review clinical data, and ensure trial compliance with regulatory guidelines. The ideal candidate should have a Medical Doctor degree, an Infectious Diseases Fellowship certification, and at least 10 years of experience as a practicing physician. The position offers flexibility for home, office, or hybrid work, along with an attractive income package and benefits.

Servicios

Performance-based bonuses

Corporate benefits

Intensive induction program

Formación

• Minimum of 10 years experience as a practicing MD.
• Ability to advise on medical matters for clinical studies.
• Experience in reviewing and analyzing clinical data.

Responsabilidades

• Advise clients and teams on medical matters.
• Collaborate in preparing clinical development plans and reports.
• Ensure accuracy and compliance of trial data.
• Identify and mitigate trial risks.

Conocimientos

Full working proficiency in English

Communication skills

Presentation skills

Analytical skills

Problem-solving

Detail-oriented

Team-oriented

Educación

Medical Doctor degree

Infectious Diseases Fellowship certification

Herramientas

MS Office applications

Descripción del empleo

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.

Home-Based or office based/hybrid in Madrid or Barcelona

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