Medical Monitor (Board-Certified Oncologist) - Remote

Posted 2 weeks ago

Medical Monitor

Overview

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.

In Short

Advise clients, project teams, sites, data safety monitoring boards, 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
Review listings for coded events to verify Medical Dictionary for Regulatory activities
Participate in bid defense meetings
Assist in Pharmacovigilance activities
Identify Program risks, and create and implement mitigation strategies with Clinical Operations
Ability to organize and lead clinical development advisory boards and safety monitoring boards
Ensure Study team compliance with FDA, EMEA, ICH and GCP guidelines
Review and sign off clinical documents with respect to medical relevance.

Requirements

Medical Doctor degree required
Board Certification in Oncology required
Experience as a practicing Oncologist (minimum of 10 years)
Clinical Research experience required, such as experience as a Principal Investigator or Sub-Investigator
Full working proficiency in English
Proficiency with MS Office applications
Excellent communication and presentation skills, comfortable public speaking
Problem-solving, team and detail-oriented