TRABAJO ASSOCIATE REGULATORY SUBMISSIONS MADRID, MADRID

Answer quality and regulatory enquires from european competent authorities... demonstrated leadership and rapport in working with regulatory bodies... com/company/lifestyles-healthcare/...

Job description the senior associate, regulatory intelligence and analytics is responsible for completing regulatory deliverables based on an established regulatory...

Ensure regulatory compliance... maintain updated lists & tables shared with other departments new and existing products prepare and submit regulatory submissions...

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...

Previous experience in clinical trial regulatory submissions...    job description the specialist/senior specialist, study start up and regulatory is responsible...

• ensure data quality regular checks and ensure the timely provision of all information required for regulatory reporting 2... the proposed position is within the...

It provides front-line advice to all parts of the ebury group on legal, regulatory and governance matters which contribute to ebury’s growth every day...

• regulatory compliance and dialogue (e... senior consultant / associate / engagement manager... finance & risk - senior consultant / associate / engagement...

Collaboration with different departments to ensure regulatory compliance...    responsibilities your role as associate legal counsel will involve: legal advice...

Experience in managing external service providers and knowledge of quality standards and regulatory requirements... monitor implementation of the quality plan and...

Senior clinical research associate iqvia is the human data science company oriented to drive human health outcomes forward... your responsibilities will include:...

Responsibilities your role as accounting associate will involve:  review and analysis of all balance sheet accounts and income statements...

Support regulatory team in preparing documents for study submissions... job description as a clinical research associate i you will work on the frontline of communication...

This includes agreeing exceptions noted with stakeholders and drafting of audit findings, proactively develop and maintain professional working relationships with...

Responsibilities:participate in the month-end, quarter-end and year-end closing processes, and provide support in the financial reporting process in compliance with...

Role responsibilities participate in the month-end, quarter-end and year-end closing processes, and provide support in the financial reporting process in compliance...

G pv, regulatory affairs activities... manage submissions of mif/ocabr for plasma products in loc spain/portugal... manage submissions of import/export permits for...

Desirable skills: direct experience with medical device development life cycle processes, regulatory submissions and relevant standards such as iso and iso...

• basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i... • manage the progress of assigned studies by tracking regulatory...