This position is no longer open for applications

Our client is an expanding mid-sized CRO who's looking for several Regulatory Submissions Coordinators for their office in Madrid. If you're a junior clinical research professional that wants an opportunity to work on one of the top companies in the world this is your chance. 

The role is office based in Madrid with the possibility to work 8 days per month homebased after 6 months and you don't have to travel at all. They also review the workload periodically to make sure that you have a good work-life balance. 

Responsibilities:

• Prepare, review, and file clinical trial applications for Spain;
• Provide insightful input on regulatory submissions documents and timelines;
• Ensure submissions comply with applicable regulations and guidance documents;
• Advise on changing country regulations and compliance requirements;
• Track submissions and ensure timely filing of documents.

What they're looking for: 

• At least 1 year of experience within regulatory affairs in clinical research 
• Hands-on experience preparing, reviewing, and submitting regulatory documentation
• Fluent in English and Spanish 

What they're offering: 

• Permanent position with a flexible start date
• Great training and onboarding program
• 4 opportunities of promotion per year 

Apply and send your CV to: S.Urda@nonstopconsulting.com or feel free to contact me for a confidential conversation on: +34 932 420 346 Internal Extension: 3374

 NonStop Consulting is one of the largest and fastest growing specialised life-sciences & Med-tech 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, Switzerland, Romania, Luxembourg, US and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover.