- Genentech (Boston, MA)
- …early in study designs and development programs, aligning with regulatory and scientific best practices + Partner closely with senior leadership across PD-DSA, ... clinical development, regulatory affairs , and data science teams to shape the future...in therapy area-level governance / Development Boards to ensure scientific rigor in study design, analysis, and interpretation +… more
- Astellas Pharma (Northbrook, IL)
- …conferences, is a committee member, organizes programs and sessions, chairs scientific sessions, and makes presentations. + Constantly publish manuscripts in ... + Mentor statisticians and analytics professionals across QSEG, supporting scientific development. + Share knowledge, best practices of novel methodology,… more
- J&J Family of Companies (Cincinnati, OH)
- …with products. + Cross-Functional Collaboration: Work closely with R&D, Regulatory Affairs , and supply chain partners to integrate toxicology insights into product ... staffing needs to deliver innovative product development solutions. + Scientific Communication: Prepare and present reports, presentations, and regulatory… more
- Medtronic (Mounds View, MN)
- …opportunities + Partner with marketing, geographies, clinical, legal, regulatory affairs , packaging and labeling, sales force, supply chain, documentation control, ... a minimum of 5 years of technical, medical or scientific writing/communications experience + Or Masters degree with a...a minimum of 3 years of technical, medical or scientific writing/communications experience + Or PhD with minimum of… more
- University of Southern California (Los Angeles, CA)
- …reports and presentations + Presenting findings at regional or national scientific meetings + Mentoring or overseeing biostatisticians and graduate students + ... Contributing to the writing of scientific manuscripts and grant proposals + Collaborating with team...is to be filed with the Office of Postdoctoral Affairs . REQ20166736 Posted Date: 09/03/2025 - Thru date -… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …of clinical research experience. + Or two years of college in a scientific , health related or business administration program and five years of clinical research ... clinical research experience + Or bachelor's degree in a scientific , health related or business administration program and three...+ Or master's degree, MD or PhD in a scientific , health related or business administration program and one… more
- Stony Brook University (Stony Brook, NY)
- …the collected data + Participate/assist in manuscript writing for publication in scientific journals and/or presentations. May also assist in grant writing + Lab ... + Other duties as assigned, which may include attending Scientific Conferences and Meetings **Senior Postdoctoral Associate:** **Required Qualifications:** Doctoral… more
- RELX INC (Raleigh, NC)
- …advises the RELX corporate functions and its business divisions (Legal, Risk, Scientific Technical & Medical, and Exhibitions) on various legal and compliance ... include the global procurement team, human resources and benefits, government affairs , and other corporate function teams. + Drafting, negotiating agreements and… more
- J&J Family of Companies (Titusville, NJ)
- …Clinical Development & Research - Non-MD **Job Category:** Scientific /Technology **All Job Posting Locations:** Allschwil, Switzerland, Beerse, Antwerp, ... interactions includes individuals from TA strategy, GCSO, global regulatory affairs , project management, finance, legal, quality assurance, quality monitoring &… more
- Bristol Myers Squibb (Princeton, NJ)
- …deadlines. **Education / Experience Requirements** + Bachelor's degree required; advanced scientific degree preferred (Masters, PhD, PharmD, BSN, etc.) with at least ... 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements**...globally for drug development and approval. + Understanding of scientific content and complexities and good knowledge of drug… more