- Stony Brook University (Stony Brook, NY)
- Clinical Research Associate I...clinical research trials; collect and submit clinical trial patient data , coordinate patient appointments. ... experience. Experience working with study participants. Experience with data analysis, data collection and electronic database...of posting.** **Job Number:** 2500123 **Official Job Title:** : Clinical Research Associate I **Job… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: The Clinical Research Associate I will be responsible for the coordination of clinical research studies within the Department of ... and conduct follow up research appointments for clinical trial participants, data collection and entry into paper and electronic databases. Maintenance… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: A Clinical Research Associate I will have a detailed understanding of each study protocol and background knowledge of the study medication and ... instruments; monitoring patients closely for any associated adverse events. + Maintain clinical research records; maintain files of approval letters and annual… more
- Touro University (Hawthorne, NY)
- …adverse event management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team. Responsibilities ... clinical team. + Ensure compliance with the Good Clinical Practice guidelines in clinical research...clinical team and report as required. + Enter data on Hematology, Oncology and Stem Cell Transplant patients… more
- SUNY Upstate Medical University (Syracuse, NY)
- …ship lab samples. Schedule and conduct follow up research appointments for clinical trial participants. Data collection and entry into paper and electronic ... Job Summary: Coordination of clinical research studies. Performance of regulatory tasks including IRB and sponsor/CRO regulatory correspondence. Communication… more
- IQVIA (New York, NY)
- …in lieu of degree. Req * Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. * ie, Good Clinical Practice (GCP) ... that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations...and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- SUNY Upstate Medical University (Syracuse, NY)
- …experience or equivalent combination of education and experience, experience with clinical research protocols, knowledge of medical terminology, computer skills, ... written/oral communication and organizational skills required. Preferred Qualifications: Previous clinical research experience with cardiology patients and SOCRA… more
- SUNY Upstate Medical University (Syracuse, NY)
- …screen patients for clinical research trials; collect and submit clinical trial patient data . Perform various administrative duties, which may include ... proper collection and shipment of lab samples; billing support; maintenance of clinical research study supplies and drug accountability. Minimum Qualifications:… more
- SUNY Upstate Medical University (Syracuse, NY)
- …of education and experience. SoCRA certified or ACRP certified Experience with clinical research protocols, knowledge of medical terminology, computer skills, ... Job Summary: Position is Project Manager for a large multi-site clinical trial. Train and oversee CRA's on the project. Clinical Site is also Coordination Center… more
- SUNY Upstate Medical University (Syracuse, NY)
- …and experience. Preferred Qualifications: Two years of experience in a cardiology clinical research . Work Days: M-F Daytime Hours Message to Applicants: ... and processing blood specimens, monitoring grant expenditures, proper reporting of medical data for research protocols, maintaining research documents and… more