- SUNY Upstate Medical University (Syracuse, NY)
- …and their staff to facilitate and monitor the conduct of multidepartment clinical studies . + Collaborates with principal investigators and other departmental ... or contacts based on study calendar and protocol. + Performs study related tasks, including patient interviews, clinical data collection, specimen collection… more
- Sumitomo Pharma (Albany, NY)
- …clinical programs, ensuring that the design, implementation, and conduct of the clinical studies provide unambiguous data and information that allows for ... data to regulatory agencies (FDA, EMA) during IND submissions, clinical study reports, and NDA/MAA filings. + Collaborate with regulatory affairs team… more
- SUNY Upstate Medical University (Syracuse, NY)
- …facing role, the candidate needs the ability to communicate directly with study volunteers, collecting detailed clinical information and communicating that to ... Job Summary: The Clinical Research Associate I (CRA I) will join...trials. The role will be expected to manage 2-3 studies simultaneously. The will ensure compliance with FDA guidelines… more
- Sumitomo Pharma (Albany, NY)
- …Data Manager. The ** Clinical Data Manager (CDM)** is responsible for leading a study and support complex studies . They will work closely with senior staff ... in providing support and guidance to junior staff and peers to meet study deliverables within the ICH/GCP guidance. + Perform all in-house DM activities, including… more
- Mount Sinai Health System (New York, NY)
- …is seeking a highly motivated clinically trained post-doctoral fellow to conduct clinical and translational research!** The Icahn School of Medicine at Mount Sinai ... seeking a highly motivated clinically trained post-doctoral fellow to conduct clinical and translational research in psychosis spectrum disorders or mood disorders.… more
- Actalent (New Hyde Park, NY)
- …a subject/patient-facing position, strong communication skills are essential for collecting detailed clinical information and sharing it with the study team. The ... SR CLINICAL RESEARCH COORDINATOR Job Description We are seeking...subject's schedule for compliance with the protocol. + Attend study meetings both internally and externally. + Train the… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …Ensures safety of the drug, including the safety aspects of patients in clinical studies and signal detection from post-marketing surveillance, with the support ... team. Provides input to key external presentations. + Ensures quality of all clinical documents (eg, Investigators' Brochure, protocol, study report, clinical… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …+ Serves as lead drug supply manager of multiple small and/or less complex clinical studies for the functional area in supply planning, including demand ... applies to internally sourced studies and/or CRO/Partnered studies . Collaborates and interacts with clinical trial...Manages supply planning and timelines to ensure alignment with study plans and timelines and overall clinical … more
- Mount Sinai Health System (New York, NY)
- …retrieval of documents. + Obtains and maintains required regulatory documentation and study specific regulatory binders for all studies . **Document Collection ... Regulatory Assistant II plays a vital role in supporting clinical research compliance by managing and maintaining electronic regulatory...all other related duties as assigned. + Prepare for study monitoring and auditing visits with study … more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …Ensures safety of the drug, including the safety aspects of patients in clinical studies and signal detection from post-marketing surveillance, with the support ... from Global Patient Safety. + Ensures quality of all clinical documents (eg, Investigators' Brochure, protocol, study report, clinical components of… more