- Lilly (Indianapolis, IN)
- …who need them all over the world. The Senior Advisor/Director Post approval scientist in Global Regulatory Affairs - CMC commercial solid oral products ... strategies and submissions for Lilly's commercial solid oral products. The regulatory scientist will be encouraged to demonstrate innovative regulatory… more
- Veterans Affairs, Veterans Health Administration (Murfreesboro, TN)
- …EDRP application. Responsibilities The incumbent is a Supervisory Clinical Laboratory Scientist (Laboratory Manager) serving in the department of Pathology and ... program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Qualifications Applicants pending the...next lower grade level (GS-12 / Lead Clinical Laboratory Scientist ), which is directly related to the position to… more
- Cambrex High Point (High Point, NC)
- …world. Start a career where You Matter by applying today! Job Overview The Senior Scientist , Regulatory Compliance will provide oversight of regulatory ... GXP/QA/ regulatory compliant pharmaceutical laboratory environment or Quality Assurance/ Regulatory Affairs role (prefer late phase/commercial experience).… more
- Merck (Austin, TX)
- …+ Coordinate regional regulatory strategy and submissions through collaboration with Regulatory Affairs Europe (RAE) and local affiliate teams. + Provide ... + Local registration study protocols for secondary markets + Represent Global Regulatory Affairs on internal committees (eg, DRC, ADT/PDT, EDT, LEAD) to provide… more
- Lilly (Indianapolis, IN)
- …medicines to patients who need them all over the world. The Advisor Post approval scientist in Global Regulatory Affairs - CMC Commercial Products will ... regulatory strategies and submissions for Lilly's commercial products. The regulatory scientist will be expected to demonstrate innovative regulatory… more
- Lilly (Indianapolis, IN)
- …life-changing new medicines to patients who need them all over the world. The Senior Advisor/Director in Global Regulatory Affairs - CMC Pre-approval Small ... the synthetic molecule portfolio, including small molecules, peptides, and oligonucleotides. The regulatory scientist will be expected to leverage innovative … more
- Abbott (Plymouth, MN)
- …teams, including Marketing, R&D, Field Operations, Risk Management, Reimbursement, Medical Affairs , Quality, and Regulatory Affairs . You will ... Program Management, Reimbursement, Medical Affairs , Risk Management, Quality and Regulatory Affairs , and investigational sites. + Oversee study Steering… more
- Merck (Boston, MA)
- …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations) + ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… more
- Danaher Corporation (Sunnyvale, CA)
- …System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Senior Clinical Research Scientist reporting to ... commercialization of products. This position is part of Clinical Affairs and will be an Onsite Role in Sunnyvale,...will be an Onsite Role in Sunnyvale, CA. The senior clinical research scientist will work on… more
- Merck (North Wales, PA)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The Senior Director ( Senior Principal Scientist...Pulmonary Disease Research, Pulmonary Disease Treatment, Pulmonary Disorders, Pulmonology, Regulatory Affairs Compliance, Regulatory Compliance,… more