CLINICAL DATA SPECIALIST

Job Responsibilities:

Determine and direct the program level strategy for data related activities for
global drug development programs. Programs may be in one or more stages of drug
development Early Discovery, Full Development, and LifeCycle Management
requiring interaction with different teams and operating models. Colead the
multidisciplinary team responsible for setting the program level data
collection, handling, and review standards and timelines for the program.
Provide oversight to ensure consistency, timeliness, and quality of data review
across the protocols in the program. Also responsible for providing data
management expertise to the program and mentoring of data managers with regard
to data management policies and procedures and drug program project management.

Job Requirements/Education:

Minimum of Bachelors degree with 5-10 years experience in pharmaceutical
industry of which 5 years have been in Clinical Data Management. Experience in
the conduct and management of multiple concurrent clinical trials, designing
case report forms and other data documents, reviewing and cleaning trial data,
and locking databases. Demonstrated ability to lead multidisciplinary teams and
build alignment across functional areas. Strong negotiation and collaboration
skills with ability to drive resolution of complex issues. Broad experience
using various relational database tools and applications for data retrieval,
error detection, listings, and production of standard displays. Experience in
project planning and management including resourcing, risk assessment and
management, and timeline projections. Excellent communication skills both
verbal and written. Experience working in a team environment within a matrix
organization

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