Clinical Trial Application Submission Manager

Are you looking for a new Regulatory CTA submissions contract?  Are you looking to work within a Global team of other likeminded Regulatory Affairs professionals?  If so, please take a look at this new and exciting project below.

We are looking for candidates to join at the beginning of May to join our client on an 8 month basis.

This position is responsible for managing regulatory Clinical Trial Applications (CTA) submission activities for assigned clinical trials (Phase 1 - Phase 4 spanning five therapeutic areas Oncology, Neuroscience, Cardiovascular and Metabolism, Immunology, and Infectious Disease).
 

The Regulatory Clinical Trial Application submission manager has experience in regulatory CTA submission regulations, requirements and will be responsible for the execution of the global CTA submission strategy, as well as the quality and completeness of the CTA regulatory submissions for Clinical Trial Applications, throughout the lifecycle of the trial.

 
Successful candidates for this position have: in depth regulatory submission experience and regulatory knowledge, project management and leadership skills and strong communication skills.

We are able to offer candidates a very competitive rate and the chance to work within a superb team.

If you feel that this may be of interest to you, please do not hesitate to contact me.




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