TRABAJO REGULATORY AFFAIRS MANAGER CLINICAL 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...

¿qué buscamos? estamos en la búsqueda de un regulatory manager que comparta nuestra visión y esté listo para contribuir a proyectos desafiantes...

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...

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

Due to our constant growth, we are looking for a regulatory affairs specialist to support our projects in our office in madrid (spain)you will be responsible for:execution...

Maintain knowledge of industry, company, and regulatory guidelines... within integrated data analytics & reporting (idar), the regulatory medical writing team are...

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

Angel) ensuring compliance with the astrazeneca authoring guide for regulatory documents... • coordinates administrative tasks during the study process, audits and...

Ensure regulatory compliance (ce mark, fda) for the medical device platform, coordinating with qa and clinical teams... role overview:we are seeking an experienced...

Key responsibilities: clinical excellence: promotes clinical excellence by educating others on the importance of incorporating in-depth clinical, procedural, and...

Description: is the leader of the project team and responsible for collaboration with assigned team in meeting client deliverables as outlined in the contract responsible...

Advanced knowledge of federal regulations, good clinical practice, and good clinical data management practices... this unique role within iqvia lends itself to a...

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

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

Plans, organizes, and prioritizes own daily work routine to meet established schedule with guidance from manager... support employees/customers by providing clear...

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