Provides all levels of medical monitoring activities including patient safety surveillance and integrity.
Included in multi-cross-functional support to the project team in conducting clinical trials
Could act as the main point of contact with the sponsor as a medical representative
Coordination and delivery of trainings, supervision, and oversight of Medical Monitors
Main point of contact and escalation for Medical Monitors
Participation in the development and revision of Medical Monitoring SOPs
Assists with the assignment, transitioning, and assimilation of individuals to work as Medical Advisors, Medical Monitors and Study Physicians on project.
Interacts with other departments to ensure the required quality of service is provided to a sponsor

Proven, efficient medical communication
Highly organized, with strong interpersonal, presentational, and documentation skills
Proven efficiency in timely delivery
Self-motivated, able to work independently, as well as in multi-disciplinary teams, and with the intellectual flexibility to continually develop and learn new skills
In-depth knowledge of medical terminology and of GCP, ICH guidelines relevant to global drug safety and drug development process and regulations
Good decision-making and problem resolution based on all relevant information.
Strategic thinking, recognizing key issues and providing practical solutions
Ability to work effectively in an environment characterized by tight timelines and changing priorities.
Excellent Leadership skills

Training and career development opportunities internally
Strong emphasis on personal and professional growth
Friendly, supportive working environment
Opportunity to work with colleagues based all over the world, with English as the company language

Medical Director – Senior Medical Monitor, Extensive Oncology Experience Required

Key skills