- Otsuka America Pharmaceutical Inc. (Boise, ID)
- …quantitative field. + 7+ (PhD)/10+ (masters) years' experience in pharmaceutical/biotechnology/ CRO industry. + Strong statistical background demonstrated by serving ... in primary roles as statistician or lead statistician in trial design and analyses. + Experienced in developing statistical analyses plans and possesses a strong interest to learn and develop novel statistical and epidemiological methods to support evidence… more
- Charles River Laboratories (Rockville, MD)
- …**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
- Charles River Laboratories (Shrewsbury, MA)
- …(SOPs). * Review documentation of functions performed as part of quality control requirements. * Perform quarantine & isolation procedures as they relate to ... **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
- Abbott (Alameda, CA)
- …forms (CRFs), conducting User Acceptance Testing (UAT), Contract Research Organization ( CRO ) selection and management, selection and training of investigator sites, ... planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions. + Maintain and audit Trial Master File to ensure inspection readiness. + Perform review of clinical data listings for… more
- Beth Israel Lahey Health (Burlington, MA)
- …reorders as necessary. 7) Maintains a professional relationship with sponsors and/or CRO 's and related members: + Maintains regular and appropriate communication. + ... Works with sponsor monitors during monitoring visits; promptly responds to sponsor requests for additional material, clarifying material or missing material. + Works cooperatively with sponsor to ensure that good clinical practice are being followed. +… more
- Charles River Laboratories (Charleston, SC)
- …**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
- Charles River Laboratories (Worcester, MA)
- …**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
- Adecco US, Inc. (Cambridge, MA)
- …development of small-molecule oral dosage forms. + Implement **product control strategies** and provide technical support for significant manufacturing deviations. ... Draft technical reports supporting life cycle management, regulatory submissions, and product control . + Support MSAT Program Directors and CMC Leaders by planning,… more
- Community Based Care of Brevard, Inc. (Rockledge, FL)
- …rr ed Physical Re quirements: Gr as pi ng Reaching Sitti ng Stand i ng Sto o pi ng / Cro uch i ng Be nd i ng Reading Sp ea k ing Listening Ty p ing Writing No ise Co ... nd itio ns Work in Conf in ed Spaces Family Partnerships of Central Florida is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin,… more
- AbbVie (North Chicago, IL)
- …educational equivalent & 5 years of clinical data management experience in a pharmaceutical, CRO or biotech company. Of the experience required, must have 5 years: + ... conducting phase 2 to 3 of biologics or chemical compound studies; + using the following tools daily: EDC, eCOA, IRT, CDR, SDTM, data visualization tools, risk based management & TMF; & + applying clinical trial processes, including FDA & EMA regulatory… more