Medical Monitor (Infectious Diseases).

PSI; Paris; Hybride; EUR 70 000 - 90 000; Plein temps

Résumé du poste

A leading medical consulting company seeks a Medical Monitor to provide critical medical input to clinical studies, ensuring participant safety and compliance with regulations. Candidates need a Medical Doctor degree with a specialization in Infectious Diseases and at least 10 years of clinical experience. The position offers a supportive and international work environment, flexible work options, and an attractive compensation package including performance-based bonuses.

Prestations

Performance-based bonuses

Corporate benefits

Industry-related training

Qualifications

• Minimum of 10 years of experience as a practicing MD.
• Communication, presentation and analytical skills are essential.
• Proficiency in English is required.

Responsabilités

• Advise clients and teams on medical matters.
• Collaborate on clinical development plans and reports.
• Review clinical data for participant safety.
• Ensure compliance with protocols and guidelines.
• Address safety issues from sites and the team.

Connaissances

Communication skills

Analytical skills

Problem-solving

Team-oriented

Detail-oriented

Full working proficiency in English

Formation

Medical Doctor degree

Infectious Diseases Fellowship certification

Outils

MS Office applications

Description du poste

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 France

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