Project Specialist with experience in global clinical trials and solid foundation of regulatory documentation compliance. Effective communicator with multinational background. Driven and compassionate about finding positive outcomes in healthcare.
billing, clinical study, clinical trials, coach, content, credit, client, clients, database, diagnosis, documentation, Electronic Medical Records, feasibility study, feasibility studies, financial, Forms, French, GCP, German, government regulations, insurance, legal, notes, Meditech System, Mentor, monitors, Communicator, policies, Polish, pricing, processes, Recruitment, Regulatory Affairs, regulatory documents, research, Russian, sales, scheduling, symposium, translation, translations
Resumes, and other information uploaded or provided by the user, are considered User Content governed by our Terms & Conditions. As such, it is not owned by us, and it is the user who retains ownership over such content.
Many factors go into creating a strong resume. Here are a few tweaks that could improve the score of this resume:
Job Titles Held: