Search Jobs: Results: Sr. Manager/Manager - GLP Tox

Now is an exciting time to join a rapidly expanding clinical stage pharma. The company thrives in a fast-paced, collegial environment, with multiple drugs in development from pre-IND up through Phase 3 (in multiple therapeutic areas).

 

There is an immediate need to bring on board someone who has at least 2-5 years of pharma industry experience who has a strong GLP tox background (either a previous tox Study Director in a CRO with GLP experience or pharma industry experience working with external CROs to manage GLP tox).

 

This client is seeking someone who can step in one day one and contribute and provide the leadership for studies being outsourced at CROs.

 

Must have previous pharma industry experience with design of study protocols and the ability to interpret data from safety studies.

 

Excellent communication skills required. Ph.D. preferred, but MS or BS level may be considered depending on experience level.

 

Must be able to travel up to 25% (monitoring external tox studies)


Job Details

Name:   Joanne Gehas   Date Posted:   06/22/2017
Office:   Raleigh   Telephone:   (919) 760-3005
Email:   jgehas@fpcraleigh.com   Fax:   (919) 848-1062
Industry:   Biopharmaceutical /Biotechnology, Pharmaceutical
Function:   Sciences   Sub Category:   Scientist, ...»
Keywords:   GLP, toxicology, regulatory, IND, clinical, protocols, CRO   Region:  
State:   Massachusetts   City:  
Education:   BS, MS, PhD   Job Number:   J53735-RALE

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