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
All your information will be kept confidential according to EEO guidelines.
Sr. BA - Clinical operations • Rockville, MD, United States
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