- ThermoFisher Scientific (Wilmington, NC)
- …expert for study design, adverse event reporting, and interpretation of statistical data . . Stay current with ICH, FDA, and global regulatory guidance. Represent ... writing experience, including at least 2 years in medical writing within pharma/ CRO and 1+ year of leadership responsibility. . Exceptional writing, editorial, and… more
- Charles River Laboratories (Mattawan, MI)
- …each area's training plan and business needs. + Collect, document, review, and verify data on forms, or in electronic data capture systems. + Review ... documentation of functions performed as part of quality control requirements. + Use and maintain instrumentation and equipment. + Perform all other related duties as… more
- Eurofins US Network (Des Moines, IA)
- …or as needed for quality control tests or regulatory purposes. 10. Record test data and results for samples in logbook, record book or BookMaster and enter the ... pharmaceuticals and cosmetics testing as well as in agro-sciences CRO (Contract Research Organization) services. **Job Description** On Call/Flex...data or results into eLIMS either manually or through… more
- PsychoGenics (Paramus, NJ)
- Research Associate 1 **PsychoGenics** is a preclinical CRO with expertise in central nervous system (CNS) and orphan disorders. Our mission is to provide the best ... temporal and vectoral datasets (more than half a million data points per mouse per session). The SmartCube platform...and formulation + Compound dosing (IP, SC, PO) + Data handling and analysis + Tissue collection + Assist… more
- Insight Global (Lower Gwynedd, PA)
- …accurate documentation in Electronic Lab Notebook (ELN). * Conduct first-pass data analysis and summarize findings. * Collaborate with translational science leads ... and documentation skills. o Ability to analyze and interpret experimental data . o Excellent verbal communication and team collaboration. Preferred Background *… more
- Otsuka America Pharmaceutical Inc. (Lansing, MI)
- …budget forecast to the Director/Associate Director. * Establish communication flow with CRO and investigative sites to maximize compliance with study protocol. * ... as assigned. * Participates in ongoing review of clinical trial data focusing on data integrity, trending and consistency. * Supports project level inspection… more
- University of Miami (Coral Gables, FL)
- …administration, departmental research support, independent research site, sponsor or CRO , ideally in an academic setting. Appropriate combination of relevant ... development process strongly preferred. + Skill in collecting, organizing, and analyzing data . + Ability to recognize, analyze, and solve a variety of problems.… more
- Sanofi Group (Cambridge, MA)
- …4 years experience in clinical development in the pharmaceutical industry, CRO , or healthcare institution **Soft skills** + Excellent communication skills (verbal ... + Quality-focused, adept at developing good practices, open-minded to data -driven approaches and new digital solutions + International/ intercultural working… more
- BeOne Medicines (San Mateo, CA)
- …scientific expertise for selection of investigator and vendors Train BeiGene colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or ... Authorities, and CROs Review, query, and analyze clinical trial data Interpret, and present clinical trial data ...trial data Interpret, and present clinical trial data both internally and externally Represent a clinical study… more
- Eurofins US Network (Indianapolis, IN)
- …leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders ... + Document laboratory work in notebooks/electronic notebooks and log books, perform data integrity checks, data verification reviews, and communicate final… more