TRABAJO CLINICAL REGULATORY AFFAIRS LEAD MADRID, MADRID

Member of relevant clinical sub teams (cst), clinical trial teams (ctt) and an ad hoc attendee at product development team (pdt) meetings active collaboration with...

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

Monitor and track legislation, regulatory development and the external environment, including proactively researching policies impacting bat regulatory agenda...

Knowledge of clinical trials - knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i...

Understanding of good clinical practice (gcp) standards... life sciences, clinical research, or a related discipline)... accurately update and maintain clinical...

lead in a team environment... may lead project-level/submission/indication writing teams... maintain knowledge of industry, company, and regulatory guidelines...

Good regulatory and/or technical writing skills... in-depth knowledge of clinical systems, procedures, and corporate standards... good knowledge and ability to apply...

Advanced knowledge of federal regulations, good clinical practice, and good clinical data management practices... prior experience in a data management related field...

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

G pv, regulatory affairs activities... ability to lead by influence and conflict management... lead or support local health authority communication on product quality...

Good understanding of clinical trial contract management... knowledge of applicable regulatory requirements, sops and company’s corporate standards...

Support creation and implementation of medical plans develop a strong business acumen, to be a key strategic business partner to the organisation in conjunction...

Food and drug administration (fda) and local regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments...

Senior cra - spain, madrid icon plc is a world-leading healthcare intelligence and clinical research organization... we are currently seeking a senior clinical research...

Ensure regulatory compliance (ce mark, fda) for the medical device platform, coordinating with qa and clinical teams... opportunity to innovate and lead in an exciting...

You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world... we lead global healthcare technology and boldly attack...