- Bristol Myers Squibb (Cambridge, MA)
- …maintain integrated cross-functional timelines for each asset indication within approved systems . Timelines should include scenario plans that actively manage risk, ... therapy areas. + Demonstrated experience in nearly all phases of research and drug development, including global regulatory submissions (IND/CTA through… more
- Robert Half Management Resources (Natick, MA)
- …accordance with US GAAP and relevant industry regulatory standards. + Research , analyze, and implement new technical accounting standards and pronouncements, ... support for complex transactions, including mergers/acquisitions, licensing agreements, and clinical trial arrangements. + Collaborate with FP& A, tax, and… more
- Beth Israel Lahey Health (Woburn, MA)
- …for implementing major projects to change or enhance business practices, processes and systems for HMFP. Draws on a broad understanding of HMFP practices and ... is dedicated to excellence and innovation in patient care, education, and research . As a physician-led organization, HMFP partners with 2,200+ providers to support… more
- ThermoFisher Scientific (Boston, MA)
- …Sequencing (NGS) based Oncology Companion Diagnostic (CDx) assays within the Clinical Sequencing Division. You will complete program goals from initial concept ... to support successful program execution. + Present and communicate to senior leadership routinely during Product Approval Committee (PAC) meetings and additional… more