- Charles River Laboratories (Rockville, MD)
- …Systems and Compliance is responsible for providing oversight to the Quality Management System for compliance with applicable CGMP regulations. This includes but is ... Responsible for managing the Quality System records process (Deviation, Change Control , Corrective Action and Preventive Action, Effectiveness Checks, Complaint … more
- Charles River Laboratories (Reno, NV)
- …1 is responsible for assisting the veterinarians in documentation, triage, and management of laboratory animal health cases. Also responsible for daily health ... animals (ie, place IVs, monitor fluids, etc.). + Participate in colony management (new NHP processing, TB testing, collection of biological samples, routine health… more
- IQVIA (Durham, NC)
- …get all the benefits of working for an industry leading global CRO while collaborating directly with cross-functional sponsor teams. Sponsor clients include world ... class pharmaceutical and biotech companies offering you unique opportunities to...+ Write statistical analysis plans. + Monitor internal and CRO project activities including timelines, deliverables, and availability of… more
- IQVIA (Durham, NC)
- …you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor ... clients include world class pharmaceutical and biotech companies offering you unique opportunities to...+ Write statistical analysis plans. + Monitor internal and CRO project activities including timelines, deliverables, and availability of… more
- IQVIA (Durham, NC)
- …you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor ... clients include world class pharmaceutical and biotech companies offering you unique opportunities to...+ Write statistical analysis plans. + Monitor internal and CRO project activities including timelines, deliverables, and availability of… more
- BeOne Medicines (San Mateo, CA)
- …scientific expertise for selection of investigator and vendors. + Train BeOne colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or ... clinical trial; respond to clinical questions from sites, IRBs/IECs, Health Authorities, and CRO 's + Review, query, and analyze clinical trial data. + Interpret, and… more
- Charles River Laboratories (Mattawan, MI)
- …performing detailed maintenance (PM/CM) on physical plant equipment, full automation control of facility plant equipment, and general maintenance activities as ... and compressors. * Operating Building Automation Systems (BAS) and equipment control systems. * Provides mentoring/training to other technicians with respect to… more
- IQVIA (Durham, NC)
- …get all the benefits of working for an industry leading global CRO while collaborating directly with expert cross-functional sponsor teams. Sponsor clients include ... world class pharmaceutical and biotech companies offering you unique opportunities to...+ Write statistical analysis plans. + Monitor internal and CRO project activities including timelines, deliverables, and availability of… more
- IQVIA (Durham, NC)
- …Degree + 10 years related experience, including 3 years of relevant industry ( CRO / Pharmaceutical ) and/or sales experience Req Or + Equivalent combination of ... of the Sales organization - FSP services for the Data Management , Biostatistics, Programming, Medical Writing, Lifecycle Safety, and Regulatory Affairs functions… more
- Amgen (Thousand Oaks, CA)
- …years leading or mentoring scientific staff and managing project portfolios in pharmaceutical or contract research organizations ( CRO ) setting + Hands-on ... preclinical imaging laboratory (PET, CT, MRI, and radiochemistry) and external CRO capabilities to answer critical scientific questions + Partner with multiple… more