- System One (Rochester, NY)
- …unblinded role. * Understands the drug preparation instructions and storage directions for the study drug to be administered. * Ensures study drug is ... assigned protocols as unblinded injector * Documents and tracks the drug accountability for vaccines per study and any required logs * Completes study source… more
- Stony Brook University (Stony Brook, NY)
- …IRB compliance. + Perform various administrative duties; maintenance of clinical research study supplies and drug /device accountability. + Educate families as ... (2) years of full-time clinical research experience. Experience working with study participants. Experience with data analysis, data collection and electronic… more
- Albany Medical Center (Albany, NY)
- …return required materials. + Unpack/inventory incoming study drugs and insure that study drug is placed and proper store temperature. + Organize and maintain ... assistant to the Principal Investigator. This includes: communication link between study sponsors, investigators, and institutional officials; serves as a resource… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …insights. + Generate key research questions and then design and execute studies and analyses to help address these questions, interpret the results of ... these studies and summarize ensuing insights in a variety of...leading complex human genetics research endeavors. Knowledge of different study designs and analyses including GWAS, exome or genome… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …contributing to the execution of, and interpreting large and complex human genetic studies in the therapeutic areas. We hope you are excited by the opportunity ... the following: + Applying human genetics to target discovery, selecting indications for drug programs, and identifying subgroups of patients who are more likely to… more
- Pfizer (Pearl River, NY)
- …You will be the Oncology Clinical Development expert for assigned studies maintaining current scientific and clinical knowledge. **POSITION RESPONSIBILITIES** : + ... data integrity and quality of the clinical trial(s). + Authors protocols, study level informed consent documents, and contributes to authoring of IBs, site… more
- Stony Brook University (Stony Brook, NY)
- …aspects of new PET studies , available radiotracers for clinical/pre-clinical studies , setting up study protocols with Institutional Review Board (IRB), ... Drug Research Committee (RDRC) and FDA Investigational New Drug (IND) approval, as well as PET analysis and...as collaborators outside the institution. * Oversee ongoing PET studies . * Oversee PET analysis and synthesize/interpret results for… more
- Sumitomo Pharma (Albany, NY)
- …the medical and scientific aspects of clinical trials, including protocol design, study endpoints, and data analysis. + Provide medical expertise to cross-functional ... programs, ensuring that the design, implementation, and conduct of the clinical studies provide unambiguous data and information that allows for clear decision… more
- IQVIA (New York, NY)
- …Management & Monitoring staff in the initiation, oversight, and follow-up of clinical studies . This is done in a strictly scientific, non-promotional manner, and in ... the initiation and conduct of prioritized Company clinical trials. + Supports clinicals study sites with knowledge and training on the disease, the treatment, the… more
- Pfizer (New York, NY)
- …beneficial customer-specific projects, collaborations, strategic medical partnerships, and non-interventional studies with the goal of advancing quality of care and ... educational programs, Health Outcomes Projects and Evaluations (HOPEs), non-interventional studies , and collaborations + Appropriately prioritize the needs of the… more