- Stony Brook University (Stony Brook, NY)
- …in the lab + Maintain study protocol documents and ensure compliance with all Institutional Review Board ( IRB ) and Safety policies. + Other duties ... Research Support Specialist **Required Qualifications (as evidenced by...histology and molecular biology techniques. Experience with IACUC and institutional protocols. Experience with transcriptomic bioinformatics analysis (Seurat, Scenic… more
- Actalent (Bronx, NY)
- …This role involves coordinating the preparation of study tools, collaborating with research nurses and physicians, and ensuring compliance with protocols. ... Job Title: Clinical Research Coordinator - Data Job Description We are...and flow sheets using Oncore(R), Excel(R), and Word. + Review patients' charts and medical history to confirm protocol… more
- Mount Sinai Health System (New York, NY)
- …study information. Assists in preparing grant applications and documents (for eg, Institutional Review Board , Grants and Contracts Office). ... **Job Description** The Clinical Research Coordinator assists in the daily activities of...Under Supervision of the Principal Investigator(s). + Ensure Proper Compliance with Institutional and Regulatory Requirements. +… more
- Mount Sinai Health System (New York, NY)
- …the preparation and submission of IRB applications. + Assist in research compliance activities. + Provide administrative support for meetings, recruitment ... and manuscripts. + Maintain and revise division work schedules. + Maintain research credentialing database for faculty, fellows, residents, staff and students. +… more
- Mount Sinai Health System (New York, NY)
- …study information. Assists in preparing grant applications and documents (for eg, Institutional Review Board , Grants and Contracts Office). ... **Job Description** The Clinical Research Coordinator assists in the daily activities of...compliance and contributing to the overall success of research initiatives + Additional duties include operational assistance with… more
- SUNY Upstate Medical University (Syracuse, NY)
- …guidelines. Interact and correspond with clinicians, sponsors, cooperative groups, Upstate's Institutional Review Board and regulatory agencies. Enroll, ... Job Summary: Coordinate various research trials for the Institute for Global Health,...register and screen patients for clinical research trials; collect and submit clinical trial patient data.… more
- University of Rochester (Rochester, NY)
- …amendments, and continuing reviews for IRB approval + Ensures compliance with all applicable regulatory and institutional requirements and standards ... of activities is identified **Liaison:** Serves as the liaison between cross-functional research team, study sponsors, and IRB to facilitate communication,… more
- University of Rochester (Rochester, NY)
- …training for all levels of expertise. This requires consulting with investigators, research personnel, review specialists, Board Members, and University ... and application of Good Clinical Practice standards required. + Familiarity with IRB management systems (eg, Huron Research Suite), learning management systems… more
- Bausch + Lomb (Albany, NY)
- …(GCP), clinical trials management (including site monitoring), scientific methods, research design, regulatory compliance , and clinical data management. ... established over our 170-year history. We have a significant global research , development, manufacturing and commercial footprint of approximately 13,000 employees… more
- Touro University (Hawthorne, NY)
- …pre-clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen collection and transmittal, data ... collection and management, adverse event management to ensure protocol compliance in conjunction with the PI, clinical team and...in conjunction with the PI, clinical team and clinical research nurses and team. Responsibilities + Assist in new… more