- Charles River Laboratories (Rockville, MD)
- …off-site archive facilities for data storage and retrieval, as required + Ensure the Document Control room is in order + Assist in compiling Document Control ... about. **Job Summary** The QA Specialist I - Document Control is responsible for managing all controlled GMP documentation...About Charles River Charles River is an early-stage contract research organization ( CRO ). We have built upon… more
- Bristol Myers Squibb (Princeton, NJ)
- …local study team to support the management of site relationships (may include CRO related issues). + May support Investigator Site Assessment Visits (ISAs) and Site ... and other local guidance, regulation and codes of practice related to Clinical Research and Medical Affairs + Knowledge and understanding of clinical research … more
- Charles River Laboratories (Stilwell, KS)
- …Safety Assessment facilities. **About Charles River** Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of ... systems. + Review documentation of functions performed as part of quality control requirements. + Use and maintain instrumentation and equipment. + Perform all… more
- Charles River Laboratories (Memphis, TN)
- …gene therapy breakthroughs. About Charles River Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of ... of excellence in the US and UK, we offer GMP-compliant and research -grade solutions, along with comprehensive analytical services and regulatory support. Whether… more
- Genentech (South San Francisco, CA)
- …integrate them into the country TA strategy. + Collaborate with Clinical Research Engagement Leaders (CRELs) on the creation and operationalization of the Country ... the assigned therapeutic area(s), working in close collaboration with CRELs and CRO partners to achieve timelines, quality standards, and study objectives. + Conduct… more
- Charles River Laboratories (Memphis, TN)
- …gene therapy breakthroughs. About Charles River Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of ... of excellence in the US and UK, we offer GMP-compliant and research -grade solutions, along with comprehensive analytical services and regulatory support. Whether… more
- Charles River Laboratories (Memphis, TN)
- …gene therapy breakthroughs. About Charles River Charles River is an early-stage contract research organization ( CRO ). We have built upon our foundation of ... of excellence in the US and UK, we offer GMP-compliant and research -grade solutions, along with comprehensive analytical services and regulatory support. Whether… more
- IQVIA (Durham, NC)
- …+ 12 years related experience, including 5 years of relevant industry ( CRO /Pharmaceutical) and/or sales experience Req Or + Equivalent combination of education, ... the job is located. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and… more
- IQVIA (Durham, NC)
- …as that accountable point for delivery and quality whilst maintaining financial control . You will manage cross functional teams across this global organization and ... + A minimum of 5 years' in Clinical Project Management in industry/ CRO /business experience is required in clinical drug development + and/or clinical operations,… more
- Bristol Myers Squibb (Philadelphia, PA)
- …investigators eg, Ph 3 top-line data. + Support Interventional and Non-Interventional Research (NIR) studies ( eg identification and assessment of potential study ... to any identified Adverse Events + If applicable, support CRO sponsored studies as agreed with home office medical...or PhD required + Minimum 3 years clinical or research experience in hematology OR 3 years as a… more