- Charles River Laboratories (Cleveland, OH)
- …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... review all procedures, materials, and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.). + Demonstrate… more
- Charles River Laboratories (Reno, NV)
- …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... surgical guidelines related to the care of laboratory animals including regulatory inspections. * Perform intermediate and advanced surgical procedures to include… more
- Trinity Health (Des Moines, IA)
- …They will follow established policies, procedures, protocols, standards, and regulatory requirements in executing job responsibilities as well as contribute ... Reviews and interprets providers orders to assure that the drug , dosage form, and dose is appropriate for the...depending on the work assignments and in accordance with regulatory and hospital policies. Documents patient care activities including… more
- Premera Blue Cross (Mountlake Terrace, WA)
- …and maintenance across multiple lines of business, ensuring strategic alignment, regulatory compliance, and cost-effective, clinically sound drug coverage ... and manage formulary strategies, including tier placement, exclusions, and preferred drug selections using pharmacoeconomic and utilization data. + Collaborate on… more
- Lotte Biologics USA LLC (Syracuse, NY)
- …Engineer/Scientist will support upstream cell culture clinical manufacture of biopharmaceutical drug substance produced at the LOTTE Biologics Syracuse facility. The ... resolution of complex problems associated with manufacturing of biopharmaceutical drug substance and/or newer modalities. The Engineer/Scientist will contribute to… more
- Charles River Laboratories (Reno, NV)
- …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... for study data collection. Basic understanding of SOPs, GLPs and other applicable regulatory guidelines governing the recording and review of study data. The pay for… more
- IQVIA (Durham, NC)
- …execute a wide range of pharmacometric analyses to inform clinical pharmacology and drug development decisions + Prepare or review PK/PD sections of dossiers for ... product registration and communicate with regulatory agencies. + Assess pharmacometric requirements for and ensure integration of pharmacometric information into … more
- AdventHealth (Orlando, FL)
- …technician activities. + Pharmacy Practice Completes critical medication order scrutiny, drug profile review, and patient monitoring to identify, prevent, or ... accurate, safe and timely medication therapy, and promotes cost-effective drug therapy, including actively participating in stewardship activities and restricted… more
- Norstella (Helena, MT)
- …best-in-class brands to help clients navigate the complexities at each step of the drug development life cycle -and get the right treatments to the right patients at ... we help our clients: * Citeline - accelerate the drug development cycle * Evaluate - bring the right... treatments, medical devices and what's new in the regulatory and commercial landscape. Relying on us to deliver… more
- Charles River Laboratories (Ashland, OH)
- …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... + Ability to ensure the integrity of the studies and fulfill the regulatory agencies requirements by performing the activities according to the Good Laboratory… more