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Irfa******
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Spain
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Last Update: 18.01.2019 at 12:00
Job Type
Full Time
Start
ASAP
Duration
11 Month +
Place
Madrid, ES
Country
Spain
Category
Regulatory, Quality, and Clinical
Description
Responsibilities
Prepare, review, and file clinical trial applications to domestic and international regulatory agencies;
Ensure submissions comply with applicable regulations and guidance documents;
Advise sponsors on changing regulations and compliance requirements; and
Track submissions and ensure timely filing of documents.
Qualifications
Bachelor's degree in life sciences;
Some work experience as a local Regulatory Submissions Coordinator ;
Excellent organization and communication skills;
Good English language skills;
Knowledge of Microsoft