- Charles River Laboratories (South San Francisco, CA)
- …safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space. **About ... Charles River** Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of laboratory animal medicine and science to… more
- US Tech Solutions (IL)
- …years of HEOR experience with proven high performance in the pharmaceutical industry, CRO , academia, or consulting. * Success in two or more core HEOR specialties ... (epidemiology, biostatistics, patient-reported outcomes, health services research, economics). * Proven ability to lead a portfolio of complex HEOR projects from inception to publication, with minimal oversight, while effectively collaborating with… more
- Charles River Laboratories (Foster City, CA)
- …to maintain animal housing areas or semi-rigid isolator environments, including room or facility personnel entry; personnel protective equipment use; and spraying ... safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space. **About… more
- Astellas Pharma (South San Francisco, CA)
- …+ Perform MS analysis and data interpretation for generated ADCs. + Managing CRO for analytical assays and data interpretation and recommendation for next steps + ... Participate in ADC projects, contributing to team decision-making through the analytical data you generate such as MS, SEC and HIC etc. + Contribute the creation of optimal ADC clinical candidates based on analytical data. + Serve as a Subject Matter Expert… more
- Charles River Laboratories (Mattawan, MI)
- …**About Charles River** Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of laboratory animal medicine and ... science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products… more
- Astellas Pharma (South San Francisco, CA)
- …ability to work in cross-functional, flexible and team-oriented environment + CRO management experience + Well-balanced communication skills (active & passive) in ... own language and in English **Preferred:** + Experience in antibody-related modality development especially in antibody-drug conjugates (ADCs) + Experience supporting ADC development from discovery to early CMC development + Experience in oncology research. +… more
- UTMB Health (Galveston, TX)
- …+ Works with the Office of Strategic Research Development and the CRO 's office. + Identifies new research collaboration opportunities. + Maintains tools as ... needed to facilitate duties. + Stays current on federal and state funding trends and policies and disseminates the information accordingly. + May serve as a backup to support pre-award research activities such as helping with budgets, bio sketches, and form… more
- Charles River Laboratories (Charleston, SC)
- …has deep knowledge of the pharmaceutical and personalcare products quality control testing markets including the regulatory and competitive landscape. This ... **About Charles River** Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of laboratory animal medicine and… more
- Otsuka America Pharmaceutical Inc. (Montpelier, VT)
- …writing vendors, MSL platforms, publication planning, scientific communications) + CRO / vendor contracts for medical affairs-sponsored studies (eg, observational, ... RWE, Phase IV) + Data sharing, data use and collaboration agreements + Software or SaaS contracts supporting medical platforms (eg, publication management, KOL engagement tools) + Confidentiality Agreements (CDAs/NDAs) + Engagement Agreements (MSAs, SOWs) +… more
- Otsuka America Pharmaceutical Inc. (Annapolis, MD)
- …in clinical quality assurance or GCP auditing within the pharmaceutical, biotech, or CRO industry. + In-depth knowledge of ICH-GCP, FDA, EMA, and other global ... regulatory requirements related to clinical research. + Experience auditing CROs, investigator sites, and clinical laboratories. + Strong analytical, organizational, and communication skills. + Ability to work independently and manage multiple audits across… more
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