- Stony Brook University (Stony Brook, NY)
- Clinical Research Associate I **Required Qualifications (as evidenced by an attached resume):** Licensed Practical Nurse in the state of New York. Two (2) ... Clinical Research Coordinator (CCRC). **Brief Description of Duties:** The Clinical Research Associate I would be responsible for supporting the … 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 ... data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory, processing clinical trial billing… 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 ... monitoring patients closely for any associated adverse events. + Maintain clinical research records; maintain files of approval letters and annual review… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: The Clinical Research Associate II (CRA II)will join a team of experienced coordinators and manage various research trials, including first ... with clinical documentation and HIPAA guidelines is required. Preferred Qualifications: Clinical Research Associate Certification (SOCRA or ACRP) OR… more
- Parexel (Albany, NY)
- …for candidates based in the Midwest, West Coast, Northeast & North Carolina The Senior Clinical Research Associate (Sr. CRA) is responsible for the site ... regulations + Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) + Preferred… 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 ... I will interact daily with clinicians, sponsors, IRB, regulatory agencies and other research professionals. This is a subject / patient facing role, the candidate… 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. Communication ... Data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory. Processing clinical trial billing… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: This position is responsible for the coordination of ALS clinical research studies. Performance of regulatory tasks including IRB and sponsor/CRO ... 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 ... with clinical team. + Ensure compliance with the Good Clinical Practice guidelines in clinical research . + Monitor study patients for adverse events in… 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
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