Search Jobs: Results: Senior Manager - Safety Assessment

Now is a very exciting time to join this well-funded, and rapidly expanding clinical stage pharma with multiple drugs in development (latest in phase 3).  The company is developing drugs in a wide variety of therapeutic areas (both small and large molecule).

Responsibilities include contributing to regulatory submissions and working directly with CROs on proposals to conduct nonclinical toxicology studies.  The role would also involve qualifying CROs and monitoring studies  (timelines, reviewing and interpreting data).    

 The ideal candidate must possess excellent interpersonal, verbal, and written communication skills and be able to manage multiple and varied tasks in a fast-paced environment.   

 Experience:

 At least 2 years of toxicology experience in conducting GLP nonclinical studies in the pharmaceutical industry or a CRO environment.

Previous study director experience in IND-enabling safety studies with small molecules is required.   Large molecule experience a plus!  Must have an understanding of FDA guidelines pertaining to preclinical/nonclinical safety assessments.

 

 


Job Details

Name:   Joanne Gehas   Date Posted:   06/16/2017
Office:   Raleigh   Telephone:   (919) 760-3005
Email:   jgehas@fpcraleigh.com   Fax:   (919) 848-1062
Industry:   Biopharmaceutical /Biotechnology, Pharmaceutical
Function:   Sciences   Sub Category:   Scientist, ...»
Keywords:     Region:  
State:   Massachusetts   City:  
Education:   MS, PhD   Job Number:   J52708-RALE

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