● Signaling and assessing local clinical research possibilities.
● Setting up, supervising, and co-reporting clinical studies.
● Presenting medical science information to audiences, journals, and key decision-makers.
● Coordinating advisory boards and round tables.
● Designing, setting up, and delivering accredited further training and leading medical and marketing projects.
● Providing medical and scientific input to the brand team.
● Ensuring integrity in company adherence to CGR rules on pharmaceutical products’ advertising, and promoting an interpretation of CGR rulings between the pharmaceutical industry and healthcare professionals.
Requirements
● MD.
● Knowledge of CGR and GCP guidelines.
● Good communication skills.
● Strategic and analytical flair.
● Flexible attitude.
● GCP license.
● Familiar with ICH GCP, and Iran MOH regulations on clinical trial studies.
● At least 2 years experience in clinical trial conduction.