- Takeda Pharmaceuticals (Boston, MA)
- …and Market Access, Global Evidence and Outcomes, Medica Affairs , Clinical Development, Regulatory Affairs , Biostatistics, Global Emerging Markets ... Interaction + Market Access, Pricing, Advocacy, Biostatistics, Global Evidence and Outcomes, Medical Affairs , Clinical Science, Legal, Regulatory + OBU 10,… more
- Merck (Rahway, NJ)
- …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
- AbbVie (San Francisco, CA)
- …programs under consideration. + Reviews and provides clinical operations content to clinical and regulatory documents (eg, INDs, IB, NDAs, BLAs, MAA, ... YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Clinical Operations Program Director is responsible to connect science and… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …Quality Agreements to ensure certificates are prepared accordingly + Consults with Regulatory Affairs on required documents needed for renewals and submissions, ... as provide Quality input for Validation projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions.… more
- Bristol Myers Squibb (Cambridge, MA)
- …(Masters, PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** ... and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director, Global Regulatory Strategy, Neuroscience** **Position Summary:**… more
- Merck (Providence, RI)
- …immunology, neurology, cardiometabolic and others as needed by the pipeline. + Work with Regulatory Affairs to ensure that regulatory documents (eg, IDEs, ... **Job Description** The Associate Vice President (AVP) / Companion Diagnostics will...and interact with various stakeholders to ensure alignment with clinical development timelines and regulatory requirements. Most… more
- Texas Health Resources (Plano, TX)
- The Assistant Vice President/ Associate Chief Medical Officer will provide administrative oversight and assistance with hospital's medical staff, physician ... recruitment, hospital operations and clinical programs in collaboration with Chief Quality Medical Officer...in collaboration with Chief Quality Medical Officer (CQMO). **The Associate Chief Medical Officer has the following duties and… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …Regeneron's drug development pipeline in partnership with Diagnostic Strategy Leads and IVD Regulatory Affairs . This is a leadership role within Regeneron's ... Develop and maintain project plans to closely track CDx development and CDx regulatory activities against clinical drug development and study timelines + Review… more
- BeOne Medicines (San Mateo, CA)
- …leadership team, provides strategic leadership, management, and/or mentorship to regional clinical study managers & regional clinical trial manager associates/ ... designated therapeutic area or asset + Line manager to Associate Directors in the team + Accountable for early...quality, within agreed timelines and budget + Leads regional clinical operations teams (including external partners working on a… more
- Edwards Lifesciences (New Orleans, LA)
- …assigned Regional Director and will collaborate with multiple departments including Sales, Clinical Affairs , Marketing, Quality, Regulatory , and Education. ... and Surgery. **What you will need (Required):** + An associate 's or equivalent two (2) year clinical degree in Life Sciences or related field or equivalent… more