- Stony Brook University (Stony Brook, NY)
- Clinical Research Associate I...and documentation pertaining to regulatory requirements for clinical trials. + Obtain consent from research ... Word, Excel and/or PowerPoint. **Brief Description of Duties:** At Stony Brook Medicine, a Clinical Research Associate is a valuable member of our team,… more
- Sumitomo Pharma (Albany, NY)
- …other duties as requested. **Key Core Competencies** + Ability to run a complex clinical research program with minimal direction + Extensive knowledge of ... seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director, Clinical Development - Oncology** . 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 ... 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
- Parexel (Albany, NY)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in ... regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures...part of the eTMF. + Provides feedback on any research related information including sites/investigators/competing studies that might be… 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
- 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: This position is responsible for the coordination of ALS clinical research studies. Performance of regulatory tasks including IRB and ... 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: 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
- 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)
- …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