We are one of the leading technical resource provider for Pharmaceutical & life science industries. We have 100+ employees working for major Pharmaceuticals Giants such as Merck, Novartis, BMS and Takeda. 

• Perform DM activities for in-house & outsourced trials: protocol review, CRF development, database set up activities, data validation process (including manual data review of listings), SAE reconciliation, managing local labs, external labs & database lock.
• Perform Project Management : represent DM on clinical teams, coordinate deliverables by other functions and/or CRO as necessary to achieve DM deliverables.

• Exp in Data Management w/ exp in managing projects, project teams.
• Exp w/ In-Form or other EDC software is highly preferred
• Exp w/ supporting Oncology studies.
• Proficiency on all related regulations, GCP, and Good Clinical DM Practice.
• Strong Project management skills

All your information will be kept confidential according to EEO guidelines.