Clinical Research Associate II, Ardsley, NY (Sorry, no relo avail.)
– Growing pharma, specializing in the discovery/development of innovative molecular targeted therapies, located in the Hudson Valley, seeks a degreed CRA with 2-4 years monitoring experience and must have some Oncology background. Assist the Director in the areas of study planning and implementation including protocol and CRF preparation, Informed Consent preparation/review, study site evaluation and selection, study initiation, routine study monitoring, study closure and assist in the preparation of safety and final study reports and IND annual reports. Strong working knowledge of GCP and ICH guidelines, regulatory requirements and QA procedures. Will assist with the planning, coordination and description of clinical drug and non-clinical study supplies. Participate in site selection, study implementation and ongoing study management of study sites via CROs. Up to 50% travel.
If you are qualified and interested – Please send me your resume and a message: CL@BonaFideStaffing.com