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:
Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelinesAdvise clients, project teams, sites, regulatory agencies and third-party vendors on medical mattersCollaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentationsReview and analysis of clinical data to ensure the safety of study participants in clinical trialsEnsure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is...