- EMCOR Group (Manchaca, TX)
- …bulk chemical systems for semi-conductor manufacturers, high-tech fabrication, pharmaceutical companies, medical complexes, and other highly specialized facilities. ... and tax rates are communicated timely and accurately. + Review contracts and leases prior to execution noting billing,...of insurance and applicable subcontracts are properly maintained. + Review all credit applications or D&B reports on new… more
- Charles River Laboratories (Reno, NV)
- …international standards, and corporate policies and procedures. This individual will review protocols for compliance with all pertinent government and international ... and routine in study design. The Quality Assurance Auditor will also prepare and review Quality Assurance files prior to Sponsor site visits; ensure that QA audit… more
- ThermoFisher Scientific (Wilmington, NC)
- …project team members and supports business development activities. Provides medical review and analysis for clinical trial serious adverse events, marketed products ... + Assists in writing (interpretation of safety and efficacy data) and/or review of CSR, IND/NDA report, ICSR, signal detection reports, periodic reports, RMP,… more
- GRAIL (Durham, NC)
- …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... duties are properly performed. **Responsibilities:** + Perform routine data review , interpretation and report release for commercially offered molecular diagnostic… more
- University of Miami (Miami, FL)
- …staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . The UHealth ... and sponsor regulations, laws, and policies. + Manages the preparation and review of investigational drug products. + Responsible for clinical drug protocol … more
- Bristol Myers Squibb (Devens, MA)
- …+ Identify and propose improvements to programs, procedures, and practices. + Review manufacturing batch records or QC testing records to ensure compliance with ... approved procedures. + Review and provide feedback on documents such as forms,...quality and operational problems. + Ability to work within pharmaceutical cleanroom environments. + Experience with quality management systems… more
- Takeda Pharmaceuticals (Boston, MA)
- …write-offs. + Responsible for working with direct reports to develop and/or review the labeling implementation plan ensuring that the most up-to-date information and ... to Local Affiliates for responses to health authorities requests, review of local labeling exceptions and alignment deferrals, etc....(MSc, PhD, or PharmD) preferred. + 10+ years of pharmaceutical industry experience. This is inclusive of 8 years… more
- HCA Healthcare (Houston, TX)
- …Lead and support study results reporting by providing critical data review , interpreting and discussing scientific results, conveying complex statistical methodology ... support by attendance at relevant symposia, scientific meetings and workshops and review of key literature + Maintain strictest confidentiality + Perform other… more
- ThermoFisher Scientific (Greenville, NC)
- …level documents, including IBs, INDs, and MAAs. + Provides senior level review of routine and sophisticated documents. Provides training and mentorship for other ... client-specific processes, and leads process improvement initiatives. May also develop, Review and manage performance metrics for assigned projects. + May serve… more
- AdventHealth (Altamonte Springs, FL)
- …to medication dispensing requests, prepares medications for pharmacist final review /check, delivers checked medications, and returns unused or expired medications ... to medication dispensing requests, prepares medications for pharmacist final review /check, delivers checked medications, and returns unused or expired medications… more