(Q-301) | Regulatory Submissions Coordinator

(Q-301) | Regulatory Submissions Coordinator

31 oct
|
Importante empresa
|
Madrid

31 oct

Importante empresa

Madrid

International CRO based in Madrid (Spain), experts providing full-service clinical development services to biopharmaceutical and medical device Sponsors is looking for a Clinical Project Manager - Regulatory Submissions Manager in joining their Clinical Operations Team.



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





- A minimum of a Bachelor's degree in life sciences is required;



- Hands-on experience preparing, reviewing, and submitting regulatory documentation and contracts;

- At least one year of work experience as a Regulatory Submissions Coordinator ;

- Excellent organization and communication skills;

- Knowledge of Microsoft® Office; and

- Fluency in English.





Travel: Minimal



If you are interested, please contact me!



Send me your CV via e-mail to [email protected] or ask for Sara Peralta at the phone number 932 420 346 extension: 7180



NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Luxembourg, Switzerland, Romania, the US and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.



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