🚀 go-pugleaf

To apply for this position, please visit this Website.
http://biotech.fyicenter.com/jobs/99898636_Clinical_Research_Associate_II_in_Biotech.html
To see other BioTech job opportunities, please visit
http://biotech.fyicenter.com/
Date: 20-Jul-2006



Clinical Research Associate II

This is a lead position. The Clinical Research Associate II manages the
implementation of study protocols at research sites. Responsibilities
include but are not limited to: serving as lead CRA for clinical
studies; performing monitoring visits including site qualification,
initiation, monitoring and closeout visits; developing monitoring plan;
maintaining contact with study sites, report preparation and
communications documentation; conducting training; preparing for and
participating in Sponsor and FDA audits; managing clinical project
assistants and associates.

Required qualifications: BA/BS degree or equivalent combination of
education and experience in a medical or scientific discipline; minimum
1 year monitoring experience; significant technical, medical or
industry experience in a clinical research setting; strong
understanding of Medical Terminology, Physiology, and Pathophysiology;
working knowledge of Good Clinical Practices; strong organizational
skills; the ability to multi-task and work effectively in a fast-paced
environment; strong written and verbal communication and diplomacy
skills; professional demeanor and appearance; ability to travel 30%.

Preferred qualifications: BS in scientific discipline; 2+ years
experience in a CRO.



Thank you,
BioTech FYI Center
http://biotech.fyicenter.com/
US-MA: Clinical Research Associate II in Biotech
To apply for this position, please visit this Website.
http://biotech.fyicenter.com/jobs/99898636_Clinical_Research_Associate_II_in_Biotech.html
To see other BioTech job opportunities, please visit
http://biotech.fyicenter.com/
Date: 20-Jul-2006



Clinical Research Associate II

This is a lead position. The Clinical Research Associate II manages the
implementation of study protocols at research sites. Responsibilities
include but are not limited to: serving as lead CRA for clinical
studies; performing monitoring visits including site qualification,
initiation, monitoring and closeout visits; developing monitoring plan;
maintaining contact with study sites, report preparation and
communications documentation; conducting training; preparing for and
participating in Sponsor and FDA audits; managing clinical project
assistants and associates.

Required qualifications: BA/BS degree or equivalent combination of
education and experience in a medical or scientific discipline; minimum
1 year monitoring experience; significant technical, medical or
industry experience in a clinical research setting; strong
understanding of Medical Terminology, Physiology, and Pathophysiology;
working knowledge of Good Clinical Practices; strong organizational
skills; the ability to multi-task and work effectively in a fast-paced
environment; strong written and verbal communication and diplomacy
skills; professional demeanor and appearance; ability to travel 30%.

Preferred qualifications: BS in scientific discipline; 2+ years
experience in a CRO.



Thank you,
BioTech FYI Center
http://biotech.fyicenter.com/