- Alloy Therapeutics (Waltham, MA)
- …method development, or mRNA/pDNA manufacturing. + Author, review, and approve CRO protocols, reports, data packages, and method documentation. Documentation ... characterization. + Independently troubleshoot instrument and method issues, ensuring data integrity and project continuity. Reference Materials Development +… more
- Georgetown Univerisity (Washington, DC)
- …a portfolio of clinical trials overseen by the Clinical Research Organization ( CRO ) at Georgetown University Medical Center (GUMC). Working under the direct ... supervision of the Director of the CRO , the CRC will coordinate and oversee complex clinical...monitor study participants; conduct study visits and collect clinical data + Maintain accurate study documentation, including regulatory submissions,… more
- Merck (Cambridge, MA)
- …areas, as well as participate in relationship management of Contract Research Organizations ( CRO ). The ideal candidate will be an experienced in vitro biology bench ... the continued build of strategies, workflows, and capability builds at strategic CRO partners to support screening and external reagent generation in a rapidly… more
- CSL Behring (King Of Prussia, PA)
- …+ Oversee the CRO delivery or manage the in-house programming of data sets, outputs, and DDT files of clinical trials and integrated analysis. + Coordinating ... 15 years of experience in the biotech, pharma, or CRO industries . Preferred 5 or more years of...1964, the Americans with Disabilities Act, the Fair Labor Standards Act, and the Immigration Reform and Control Act.… more
- Charles River Laboratories (Wilmington, MA)
- …strategic sales plan to expand our NHP business within the pharma and CRO sectors. * Identify, qualify, and close new business opportunities with key decision-makers ... preclinical research services. * Deep understanding of the pharmaceutical and CRO landscape, particularly in preclinical development. * Knowledge of regulatory and… more
- Georgetown Univerisity (Washington, DC)
- …a portfolio of clinical trials overseen by the Clinical Research Organization ( CRO ) at Georgetown University Medical Center (GUMC). Working under the direct ... supervision of the Director of the CRO , the CRC will manage regulatory for complex clinical...This includes daily interaction with principal investigators, study coordinators, data managers, and clinical trial sponsors. The role also… more
- Takeda Pharmaceuticals (Boston, MA)
- …a necessary contributor to our inspiring, bold mission. **_GOALS:_** + Conduct data -driven feasibility assessments for Phase I - IV clinical studies, including ... selection, enrollment strategy, and modeling. + Use all competitive intelligence data to develop data -driven study start-up forecasts, benchmarking assumptions,… more
- Pfizer (Cambridge, MA)
- …Support execution for all FIH programs through proof-of concept + Set the clinical data review strategy, ensure quality data and conduct review of emerging ... clinical data and trends; review and query data ; present and discusse relevant data to...5 years of experience in a similar role in industry/ CRO , OR + MS and a minimum of 7… more
- Bristol Myers Squibb (Princeton, NJ)
- …programs (PK/PD/ADA) supporting clinical studies; oversee assay timelines, critical reagents, data transfers, and CRO deliverables. + Ensure readiness for ... with a major focus on Companion Diagnostics (CDx) design control , validation, and clinical enablement, and the agility to...IVDR, ISO13485, and 21 CFR 11 across lab operations, data , and vendor ecosystems - so we are inspection-ready,… more
- Pfizer (Groton, CT)
- **POSITION SUMMARY** You will be responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for ... within the assigned program. + Responsible for scientific oversight, data integrity and quality of the clinical trial(s). +...and minimum of 5 years Clinical Research experience in industry/ CRO , **OR** + MS in a relevant Science discipline… more