Clinical Site Monitor

Job Responsibilities:

Perform and facilitate time efficient pre-study initiation process. Orient site
personnel to study protocol and procedures. Monitor compliance to FDA
Regulations and BMS SOPs. Manage study site activities through frequent on site
visits and telephone contracts to monitor active studies and assure compliance
with protocols, applicable SOPs and government regulations. Prepare and submit
written reports, both monitoring and administrative in a timely and accurate
manner. Travel is required. Destinations based on study site locations in the
United States. Travel need varies and is anticipated to be 20 to 40 percent
within the United States.

Job Requirements/Education:

BS Degree in Biology or Health related fields required, MS a plus. Minimum 5
yrs clinical research experience including at least 2 yrs CRO or sponsor
monitoring experience required. Extensive knowledge of FDA regulations and
GCP’s required. The candidate will manage multiple projects, exhibit
excellent communication, interpersonal, time management and computer skills.
Must be comfortable with technology and be willing to adapt to changing
priorities.

Salary will be commensurate with experience.
Bristol-Myers Squibb is an equal opportunity employer. M/F/V/D