Closing Date: 09 Dec 16
Type: Full Time
Salary (£): Competitive
Medpace is seeking a Regulatory Submissions Coordinator/Start Up Specialist for our team in Milan.
Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team!
Our European activities are growing rapidly, and we are currently seeking a full-time, home-based Regulatory Submissions Coordinator/Start up Specialist to join our Clinical Operations team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
DESCRIPTION OF JOB DUTIES
•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
•Bachelor's degree in life sciences;
•Excellent organization and communication skills;
•Knowledge of Microsoft® Office; and
•Hands-on experience preparing, reviewing, and submitting regulatory documentation;
•At least two years of start up experience as a Regulatory Submissions Coordinator/Start up Specialist;
•Fluency in English and local language.
WHAT TO EXPECT NEXT
We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an interview.
Medpace Italy Srl
Via Giuseppe Sacchi 3 20121 Milano - Italy
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