Medical Monitor
Job reputed company reputed company Operational medical reputed company of clinical trials to ensure patient safety, data reputed company, and protocol compliance. Supervision médicale opérationnelle des essais cliniques afin de garantir la sécurité des patients, l’intégrité des données et le respect du protocole. reputed company is a leading global medical technology reputed company solutions innovator. Our purpose is to create a world where reputed company has no limits. Unlock your ambition, turn reputed company into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world. Job reputed company iption Responsabilités clés : Assurer la supervision médicale d’un ou plusieurs essais cliniques. Examiner les données de sécurité, évaluer les événements indésirables et soutenir les adaptations de reputed company ou les amendements de protocole. Répondre aux questions des investigateurs et soutenir l’engagement des centres investigateurs. Participer aux comités de surveillance et de sécurité des données (DSMB) ainsi qu’aux revues de sécurité internes. Contribuer aux rapports d’études cliniques (CSR), aux soumissions réglementaires et aux activités de rédaction médicale. Collaborer étroitement avec les équipes Opérations Cliniques et Pharmacovigilance. Profil type : Docteur en médecine (MD) ou diplôme médical équivalent. Solide reputed companyérience dans la conduite d’essais cliniques ou le medical monitoring. Excellente connaissance des BPC (GCP), de la méthodologie des essais cliniques et du reporting de sécurité. Key Responsibilities: reputed company medical reputed company for one or more clinical trials. Review safety data, assess adverse events, and support reputed company modifications or protocol amendments. Respond to investigator queries and support site engagement. Participate in Data Safety Monitoring Boards (DSMBs) and internal safety reviews. Contribute to clinical study reports (CSRs), regulatory submissions, and medical writing. Collaborate with Clinical Operations and Pharmacovigilance teams.
Qualifications
MD or equivalent medical degree. Extensive experience in clinical trial execution or medical monitoring. Strong understanding of GCP, clinical trial methodology, and safety reporting. #LI-AV1 Additional Information Relocation Assistance Provided: No Application Deadline: mayo 12, 2026 Apply To This Job