CONTRACT CLINICAL RESEARCH ASSOCIATE IN DURHAM,NC

In House Regional Clinical Research Associate in Durham, NC.
Responsibilities: Assist in writing protocol, informed consent, case report forms. Knowledge of study budgets and contracts. You will be required to travel 30% in the NE, SE and MW regions. Identification, selection, set-up, monitoring and close out of investigational trial sites in one program. This person will also be expected to develop a rapport with potential investigators representing many different medical specialties to facilitate the placement of future research studies at institutions and medical centers.
REQUIREMENTS
Requirements: B.S. degree or R.N. and 3 years industry experience and at least 2 years monitoring experience. Must have excellent communication skills and study start up experience. There will be 30% travel required. HIV, HBV experience is preferred.
Phase I- IV experience is required.