- 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 ... of duties is but not limited to: performance of regulatory tasks including IRB and sponsor/CRO regulatory ...and entry into paper and electronic databases. Maintenance of clinical research supply inventory, processing clinical… more
- Danaher Corporation (New York, NY)
- …Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Clinical Research Associate is responsible ... experience OR Master's degree with 1+ years clinical research experience + Basic knowledge of regulatory requirements and Good Clinical Practice for in… 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
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: Coordination of clinical research studies. Performance of regulatory tasks including IRB and sponsor/CRO regulatory correspondence. ... Data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory. Processing clinical trial billing… 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 ... pre- clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment,...clinical team. + Ensure compliance with the Good Clinical Practice guidelines in clinical research… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: The Clinical Research Associate I (CRA I) will join a team of experienced associates and manage various research trials, including first in ... all managed studies. The CRA I will interact daily with clinicians, sponsors, IRB, regulatory agencies and other research professionals. This is a subject /… 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 ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… 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)
- …Review Board and regulatory agencies. Enroll, register and screen patients for clinical research trials; collect and submit clinical trial patient data. ... 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