Clinical Research Associate, Regulatory Master Files

Omnicare Clinical Research is currently seeking in-house CRAs to work in our Regulatory Master Files deparment located in King of Prussia (Philadelphia suburbs). 

 

Responsibilities for this position includes: receive missing/expired Essential documents from investigator sites; manage Protocol Amendment, IND Safety report, and Investigator brochure notification; forward tracking documents to Project Management.


Qualifications:



- Associate's or Bachelor's degree.
- Clinical Research experience including experience with regulatory documents.
- High degree of accuracy and attention to detail.

- Ability to multi-task with strong time management skills; ability to maintain high level of confidentiality.

- Ability to work independently, with minimal supervision.



Omnicare Clinical Research is a global CRO that offers full-service clinical research capabilities across all therapeutic areas. Coupled with our customer-centric focus, we provide clients with exceptional service throughout all phases of drug development. Our global, integrated network of 30 offices with a presence in 27 countries provides convenient access to expertise and patients around the world.


 

 

Please forward a copy of your resume to Human Resources, Omnicare Clinical Research, 630 Allendale Road, King of Prussia, PA 19406. Careers@OmnicareCR.com .