- Stony Brook University (Stony Brook, NY)
- Clinical Research Associate I **Required Qualifications (as evidenced by an attached resume):** Bachelor's Degree (foreign equivalent or higher). Two (2) ... with grant submissions and renewals. + Attend conferences and research meetings. + Assure timely communication of regulatory...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 ... 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
- ICON Clinical Research (New York, NY)
- As a Senior Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organization, powered by ... and support to site personnel on study procedures and regulatory requirements + Monitoring complex Phase 1 oncology trials,...professional (eg, RN) is also acceptable. + An experienced Clinical Research Associate with 5+… 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 ... 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
- 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
- Stony Brook University (Stony Brook, NY)
- …at least 1-2 years of experience clinical trial monitoring/auditing, research compliance, or regulatory oversight/project management of human subject ... Director of Clinical Research Compliance and Privacy **Position...guidance to SBM leadership and staff on requirements and regulatory topics pertaining to research and academic… more