Job Description Client: Otsuka Sr. BA Location: On-site Princeton, NJ. Should be able to travel to Rockville, MD Duration: 3 to 6 months • 9-11 years of experience in a pharmaceutical company/CRO with business analyst along with project management • Strong understanding/knowledge on clinical research and development area with regulatory documentation • Strong understanding of clinical, data management, safety and regulatory IT systems such as CDMS (EDC), CTMS, eTMF, RBM, IVRS, Safety, Regulatory submission and publishing systems • Experience in end-to-end (full service) clinical trials management, ideally with project management relevant clinical research experience • Understanding of various business groups and their functions tied to clinical drug development • Experience to understand and come up plan to fill the gap between business process and technologists • Should be aware of end to end clinical business and technical process • Should be able to take a problem statement and do industry research. Come up with options / solutions available. Should be able to draft RFI/RFP – and Lead them • Bring in best practices for BAs. • Should be very good in business case preparation, road mapping etc • Should have experience as a business process consultant. • Very proactive, motivational, and can work independently • Ability to understand large complex processes with a focus on continuous improvement • Strong technical writing skills and analytical skills • Strong networking abilities and an ability/willingness to work with individuals globally Additional Information All your information will be kept confidential according to EEO guidelines.