TRABAJO REGULATORY AFFAIRS CLINICAL WRITING MADRID, MADRID

Previous experience in clinical trial regulatory submissions... knowledge of the principles, methods, and procedures of clinical research...

Receive investigator proposals for iis and ensure they are discussed within the medical affairs department for decision... description of r&d programs and discussing...

The project manager is responsible for maintaining the proper project documentation and ensuring compliance with sops and regulatory requirements for clinical...

Human science,  experience and/or training: call center, medical information, pharmaceutical industry, and clinical experiences including medical writing...

G pv, regulatory affairs activities... support regulatory surveillance and intelligence in the spanish loc for new or emerging regulations...

At ease in a clinical selling environment... quality: ensure awareness and compliance with applicable standard operating procedures to meet, comply and champion...