ASSOCIATE DIRECTOR - IXABEPILONE FDT

Job Responsibilities:

Responsible for directing the following activities for assigned clinical drug
studies. Directs the design, development and execution of clinical drug
development plans, protocols and related activities. Assures that protocols
will adhereto standard clinical practices. Designs protocols from a physicians
standpoint. Secures the conditions essential for safety, efficacy and medical
usefulness of a drug. Decides how the resulting data should be analyzed and
interpreted. Recommends new approaches to data analysis and preparation.
Develops staff of physicians, scientists, and coordinators by providing
training and guidance. Organizes meetings to discuss critical issues, such as
safety and efficacy. Participates in Project Development Teams. Coordinates
with related clinical functional areas of PRI, such as Biostatistics, Human
Pharmacology and Regulatory Affairs.

Job Requirements/Education:

Minimum of three years of relevant experience preferred. Must have demonstrated
originality in problem solving as applied to drug development. Should have
skills and experience in dealing with government officials in the US and
abroad. Board certified or eligible in oncology, hematology or equivalent.

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