ESSENTIAL TASKS:
1) Write and code logical and physical database descriptions and specify identifiers of database to management system or direct others in coding descriptions.
2) Support development of DM study documentation, including: Data Management Plans, annotated CRFs

KNOWLEDGE, SKILLS, and ABILITIES:
1) Support User Acceptance Testing of Database.
2) Support medical coding and facilitate reviews.
3) Support data cleaning activities.
4) Support DM SAS programming activities.
5) Provide DM infrastructure support as needed (i.e. policy development, Lab Normal database). With minimal oversight, develop DM deliverables including but not limited to DMPs, CRFs, CRF Completion Guidelines, Edit Checks, UAT specifications and Data Review Plans.

EDUCATION, EXPERIENCE, and LICENSES/CERTIFICATIONS:
1) Bachelor's degree in a technical field such as computer science, computer engineering or related field required. Graduate degree preferred.
2) 5-7 years of applicable experience required.
3) Previous EDC and SAS programming experience desired.
4) Strong working knowledge of MS Office. Ability to work independently and with a team.
5) The successful candidate will be self-motivated and able to multi-task effectively.
6) Strong interpersonal skills in a team environment. ICH GCP guidelines, SDTM, CDISC, database development, UAT, the drug development process. Must be Flexible, easily adapts to change, and is energized by challenges and problem solving.