Pharmacovigilance Associate

PV ASSOCIATE

COMPANY INFO:

MedFocus offers clinical research contract outsourcing and staffing specifically to the pharmaceutical, biotechnology and medical device industries.  We specialize in the nationwide recruitment of clinical trials personnel.

 

Our client is recognized as a leader in the development of new, break-through technologies, first-in-man, and extremely complex studies and is seeking to add a PV Associate to their team in Cambridge, MA.

 

RESPONSIBILITIES:

· Will be responsible for basic "PV", case entry, process and assessment

· Maintenance of adverse event database

· Work with clinical investigational sites on safety issues, documenting document and process information on serious adverse events/narratives to pharmaceutical (sponsor)/FDA

· Tracking logs and paper files

 

QUALIFICATIONS:

· Excellent communication skills.

· Good lower end drug safety role with opportunity for advancement down the road

 

EDUCATION:

· College degree in science or medical (i.e. RN)

 

MedFocus offers competitive wage and benefits packages; Health Insurance, Dental Insurance, long term disability, Holiday and Vacation Time, life insurance and 401K may be applicable.