ASSOCIATE MEDICAL DIRECTOR

Job Responsibilities:

Responsible for the overall scientific and medical leadership and coordination
of the clinical development of one or more BMS MI products, with input and
oversight of the design, implementation, execution, interpretation, and
reporting of Phase I to III clinical programs. The ideal candidate will assume
leadership of the internal BMS MI clinical development teams and interface for
relevant interaction with BMS MI regulatory, preclinical and discovery groups,
and with BMS Pharmaceuticals divisions globally. The candidate will be the
primary interface and leader for interaction and liaison with scientific
leadership and investigators, advisory boards, DSMBs and adjudication panels.
Responsible for developing and refining analysis plans and reporting of
clinical study results. Works with Clinical Operations in defining immediate
and long term resource needs, clinical plans, implementation of programs and
timelines. Provides guidance and direction to operations, functions and
programs. Responsible for adverse event assessment and reporting for assigned
Phase I to III programs. Interacts with worldwide regulatory authorities as
appropriate. Creates strategies to integrate product development with
commercialization. Builds productive relationships both internally and
externally with scientists, investigators, physicians and contractors used in
the clinical development process.

Job Requirements/Education:

Physician, MD, DO or equivalent, with clinical research experience in internal
medicine or cardiovascular medicine. Board certification in radiology, internal
medicine or cardiology, or equivalent preferred. Experience with clinical
development of one agent in cardiovascular therapeutics, devices or imaging
agents required. Three to five years of pharmaceutical industry experience in
clinical research and development. Knowledge of ICH, GCP and federal
regulations and guidelines is essential, as they apply to clinical
investigation with medical imaging agents, drugs or devices. Successful
management of design, initiation, enrollment analysis and reporting of Phase I
to III clinical programs required, with preparation and filing of regulatory
submissions and approvals desirable. Knowledge of EU and non-US regulations and
requirements for clinical study conduct highly desirable. Foreign language
skills helpful but not required.

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